rs9304638

Homo sapiens
C>G / C>T
ZNF225 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
C==0218 (6556/29976,GnomAD)
C==0244 (7128/29118,TOPMED)
C==0328 (1643/5008,1000G)
chr19:44129933 (GRCh38.p7) (19q13.31)
AD
GWASdb2
1   publication(s)
See rs on genome
1 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 19NC_000019.10:g.44129933C>G
GRCh38.p7 chr 19NC_000019.10:g.44129933C>T
GRCh37.p13 chr 19NC_000019.9:g.44634086C>G
GRCh37.p13 chr 19NC_000019.9:g.44634086C>T

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
1000GenomesAfricanSub1322C=0.374T=0.626
1000GenomesAmericanSub694C=0.420T=0.580
1000GenomesEast AsianSub1008C=0.496T=0.504
1000GenomesEuropeSub1006C=0.130T=0.870
1000GenomesGlobalStudy-wide5008C=0.328T=0.672
1000GenomesSouth AsianSub978C=0.230T=0.770
The Genome Aggregation DatabaseAfricanSub8724C=0.329T=0.671
The Genome Aggregation DatabaseAmericanSub836C=0.440T=0.560
The Genome Aggregation DatabaseEast AsianSub1614C=0.454T=0.546
The Genome Aggregation DatabaseEuropeSub18500C=0.137T=0.862
The Genome Aggregation DatabaseGlobalStudy-wide29976C=0.218T=0.781
The Genome Aggregation DatabaseOtherSub302C=0.130T=0.870
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.244T=0.755
PMID Title Author Journal
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
rs93046387.16E-05alcohol consumption23743675

eQTL of rs9304638 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 rs9304638 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 )
chr191369993013700512E068-9340
chr191369993013700512E069-9340
chr191373341213733859E07023560
chr191373392713734573E07024075
chr191373460713734753E07024755
chr191373491413735107E07025062
chr191373516813735256E07025316
chr191373531313735756E07025461
chr191373341213733859E07123560
chr191373392713734573E07124075
chr191373516813735256E07125316
chr191373531313735756E07125461
chr191372673713727021E07316885
chr191373460713734753E07324755
chr191372673713727021E08116885
chr191372742313727508E08117571
chr191372779013727865E08117938
chr191372794613728087E08118094
chr191373225813732739E08122406
chr191373296413733042E08123112
chr191373321213733300E08123360
chr191373341213733859E08123560
chr191373392713734573E08124075
chr191373460713734753E08124755
chr191373491413735107E08125062
chr191373516813735256E08125316
chr191373531313735756E08125461
chr191373613313736187E08126281
chr191373638413736564E08226532
chr191374371213744383E08233860







Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr191370055213700595E072-9257