rs1606851

Homo sapiens
G>A
ZNF385D : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0364 (10898/29928,GnomAD)
A=0357 (10399/29118,TOPMED)
A=0316 (1584/5008,1000G)
A=0364 (1403/3854,ALSPAC)
A=0374 (1388/3708,TWINSUK)
chr3:21795935 (GRCh38.p7) (3p24.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.21795935G>A
GRCh37.p13 chr 3NC_000003.11:g.21837427G>A

Gene: ZNF385D, zinc finger protein 385D(minus strand)

Molecule type Change Amino acid[Codon] SO Term
ZNF385D transcriptNM_024697.2:c.N/AGenic Upstream Transcript Variant
ZNF385D transcript variant X12XM_011534122.1:c.N/AIntron Variant
ZNF385D transcript variant X13XM_011534123.2:c.N/AIntron Variant
ZNF385D transcript variant X14XM_011534124.2:c.N/AIntron Variant
ZNF385D transcript variant X1XM_017007191.1:c.N/AIntron Variant
ZNF385D transcript variant X2XM_017007192.1:c.N/AIntron Variant
ZNF385D transcript variant X3XM_017007193.1:c.N/AIntron Variant
ZNF385D transcript variant X4XM_017007194.1:c.N/AIntron Variant
ZNF385D transcript variant X5XM_017007195.1:c.N/AIntron Variant
ZNF385D transcript variant X8XM_017007198.1:c.N/AIntron Variant
ZNF385D transcript variant X9XM_017007199.1:c.N/AIntron Variant
ZNF385D transcript variant X16XM_017007203.1:c.N/AIntron Variant
ZNF385D transcript variant X6XM_017007196.1:c.N/AGenic Upstream Transcript Variant
ZNF385D transcript variant X7XM_017007197.1:c.N/AGenic Upstream Transcript Variant
ZNF385D transcript variant X10XM_017007200.1:c.N/AGenic Upstream Transcript Variant
ZNF385D transcript variant X11XM_017007201.1:c.N/AGenic Upstream Transcript Variant
ZNF385D transcript variant X15XM_017007202.1:c.N/AGenic Upstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.620A=0.380
1000GenomesAmericanSub694G=0.700A=0.300
1000GenomesEast AsianSub1008G=0.780A=0.220
1000GenomesEuropeSub1006G=0.662A=0.338
1000GenomesGlobalStudy-wide5008G=0.684A=0.316
1000GenomesSouth AsianSub978G=0.680A=0.320
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.636A=0.364
The Genome Aggregation DatabaseAfricanSub8704G=0.607A=0.393
The Genome Aggregation DatabaseAmericanSub834G=0.710A=0.290
The Genome Aggregation DatabaseEast AsianSub1620G=0.804A=0.196
The Genome Aggregation DatabaseEuropeSub18470G=0.630A=0.369
The Genome Aggregation DatabaseGlobalStudy-wide29928G=0.635A=0.364
The Genome Aggregation DatabaseOtherSub300G=0.700A=0.300
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.642A=0.357
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.626A=0.374
PMID Title Author Journal
22072270Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.Wang KSJ Neural Transm (Vienna)

P-Value

SNP ID p-value Traits Study
rs16068519.21E-05alcohol withdrawal symptoms22072270

eQTL of rs1606851 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 rs1606851 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 )
chr32178889221789248E070-48179
chr32178966621789828E070-47599
chr32178889221789248E073-48179
chr32178889221789248E081-48179
chr32179320521793776E081-43651
chr32183130421831432E081-5995
chr32183147521831557E081-5870
chr32183130421831432E082-5995
chr32183147521831557E082-5870
chr32183162021831712E082-5715
chr32183204621832327E082-5100
chr32183248021832542E082-4885




Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr32179011521790228E067-47199
chr32179058121790878E067-46549
chr32179106321791166E067-46261
chr32179140721793179E067-44248
chr32179058121790878E068-46549
chr32179106321791166E068-46261
chr32179140721793179E068-44248
chr32179011521790228E069-47199
chr32179058121790878E069-46549
chr32179106321791166E069-46261
chr32179140721793179E069-44248
chr32179058121790878E070-46549
chr32179106321791166E070-46261
chr32179140721793179E070-44248
chr32179011521790228E072-47199
chr32179058121790878E072-46549
chr32179106321791166E072-46261
chr32179140721793179E072-44248
chr32179011521790228E073-47199
chr32179058121790878E073-46549
chr32179106321791166E073-46261
chr32179140721793179E073-44248
chr32179140721793179E074-44248
chr32179011521790228E081-47199
chr32179058121790878E081-46549
chr32179106321791166E081-46261
chr32179140721793179E081-44248
chr32179011521790228E082-47199
chr32179058121790878E082-46549
chr32179106321791166E082-46261
chr32179140721793179E082-44248