rs10406335

Homo sapiens
G>A
ZNF225 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0218 (6539/29918,GnomAD)
G==0244 (7127/29118,TOPMED)
G==0328 (1644/5008,1000G)
G==0115 (445/3854,ALSPAC)
G==0119 (443/3708,TWINSUK)
chr19:44129800 (GRCh38.p7) (19q13.31)
AD
GWASdb2
2   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 19NC_000019.10:g.44129800G>A
GRCh37.p13 chr 19NC_000019.9:g.44633953G>A

Gene: ZNF225, zinc finger protein 225(plus strand)

Molecule type Change Amino acid[Codon] SO Term
ZNF225 transcript variant 2NM_001321685.1:c.N/AIntron Variant
ZNF225 transcript variant 1NM_013362.3:c.N/AIntron Variant
ZNF225 transcript variant X3XM_005259223.3:c.N/AIntron Variant
ZNF225 transcript variant X1XM_011527285.2:c.N/AIntron Variant
ZNF225 transcript variant X2XM_011527286.2:c.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.375A=0.625
1000GenomesAmericanSub694G=0.420A=0.580
1000GenomesEast AsianSub1008G=0.496A=0.504
1000GenomesEuropeSub1006G=0.130A=0.870
1000GenomesGlobalStudy-wide5008G=0.328A=0.672
1000GenomesSouth AsianSub978G=0.230A=0.770
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.115A=0.885
The Genome Aggregation DatabaseAfricanSub8688G=0.328A=0.672
The Genome Aggregation DatabaseAmericanSub836G=0.440A=0.560
The Genome Aggregation DatabaseEast AsianSub1612G=0.457A=0.543
The Genome Aggregation DatabaseEuropeSub18480G=0.137A=0.862
The Genome Aggregation DatabaseGlobalStudy-wide29918G=0.218A=0.781
The Genome Aggregation DatabaseOtherSub302G=0.130A=0.870
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.244A=0.755
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.119A=0.881
PMID Title Author Journal
18823527A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.Abraham RBMC Med Genomics
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs104063350.000144alcohol consumption23743675

eQTL of rs10406335 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs10406335 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr194467075844670818E06736805
chr194467093344671011E06736980
chr194467104944671115E06737096
chr194461888344619034E068-14919
chr194467075844670818E06836805
chr194467093344671011E06836980
chr194460014844600194E069-33759
chr194460014844600194E070-33759
chr194461888344619034E070-14919
chr194461903744619091E070-14862
chr194461912544619165E070-14788
chr194467075844670818E07036805
chr194467093344671011E07036980
chr194467104944671115E07037096
chr194467187644671938E07037923
chr194461888344619034E071-14919
chr194467075844670818E07136805
chr194467075844670818E07236805
chr194467093344671011E07236980
chr194467075844670818E07436805
chr194467093344671011E07436980
chr194467187644671938E07437923
chr194467075844670818E08136805
chr194467093344671011E08136980
chr194467104944671115E08137096
chr194467187644671938E08137923
chr194460081644600930E082-33023
chr194467093344671011E08236980
chr194467104944671115E08237096









Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr194459804744599722E067-34231
chr194461592544616789E067-17164
chr194461680644618482E067-15471
chr194464488144646741E06710928
chr194466849844670041E06734545
chr194459781244597885E068-36068
chr194459793544597989E068-35964
chr194459804744599722E068-34231
chr194461578744615827E068-18126
chr194461592544616789E068-17164
chr194461680644618482E068-15471
chr194464474344644803E06810790
chr194464488144646741E06810928
chr194466849844670041E06834545
chr194459804744599722E069-34231
chr194461578744615827E069-18126
chr194461592544616789E069-17164
chr194461680644618482E069-15471
chr194464488144646741E06910928
chr194466849844670041E06934545
chr194459804744599722E070-34231
chr194461592544616789E070-17164
chr194461680644618482E070-15471
chr194464474344644803E07010790
chr194464488144646741E07010928
chr194466849844670041E07034545
chr194459804744599722E071-34231
chr194461578744615827E071-18126
chr194461592544616789E071-17164
chr194461680644618482E071-15471
chr194464474344644803E07110790
chr194464488144646741E07110928
chr194466849844670041E07134545
chr194459804744599722E072-34231
chr194461592544616789E072-17164
chr194461680644618482E072-15471
chr194464474344644803E07210790
chr194464488144646741E07210928
chr194466849844670041E07234545
chr194459804744599722E073-34231
chr194461592544616789E073-17164
chr194461680644618482E073-15471
chr194464488144646741E07310928
chr194466849844670041E07334545
chr194459804744599722E074-34231
chr194461592544616789E074-17164
chr194461680644618482E074-15471
chr194464488144646741E07410928
chr194466849844670041E07434545
chr194459804744599722E081-34231
chr194461592544616789E081-17164
chr194461680644618482E081-15471
chr194464488144646741E08110928
chr194466849844670041E08134545
chr194459804744599722E082-34231
chr194461592544616789E082-17164
chr194461680644618482E082-15471
chr194464474344644803E08210790
chr194464488144646741E08210928
chr194466849844670041E08234545