rs10797794

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0315 (9425/29908,GnomAD)
A=0288 (8403/29118,TOPMED)
A=0350 (1753/5008,1000G)
A=0413 (1593/3854,ALSPAC)
A=0404 (1497/3708,TWINSUK)
chr1:182888873 (GRCh38.p7) (1q25.3)
CD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.182888873G>A
GRCh37.p13 chr 1NC_000001.10:g.182858008G>A
DHX9 RefSeqGeneNG_029930.1:g.54570G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.901A=0.099
1000GenomesAmericanSub694G=0.550A=0.450
1000GenomesEast AsianSub1008G=0.426A=0.574
1000GenomesEuropeSub1006G=0.607A=0.393
1000GenomesGlobalStudy-wide5008G=0.650A=0.350
1000GenomesSouth AsianSub978G=0.660A=0.340
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.587A=0.413
The Genome Aggregation DatabaseAfricanSub8702G=0.855A=0.145
The Genome Aggregation DatabaseAmericanSub836G=0.600A=0.400
The Genome Aggregation DatabaseEast AsianSub1616G=0.435A=0.565
The Genome Aggregation DatabaseEuropeSub18452G=0.631A=0.368
The Genome Aggregation DatabaseGlobalStudy-wide29908G=0.684A=0.315
The Genome Aggregation DatabaseOtherSub302G=0.640A=0.360
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.711A=0.288
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.596A=0.404
PMID Title Author Journal
23958962Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.Gelernter JMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs107977940.000119cocaine dependence23958962

eQTL of rs10797794 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr1:182858008LAMC1ENSG00000135862.5G>A2.1129e-17-134587Cerebellum

meQTL of rs10797794 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 )
chr1182812593182812642E067-45366
chr1182812701182812741E067-45267
chr1182813060182813114E067-44894
chr1182814736182814780E067-43228
chr1182815161182815267E067-42741
chr1182824393182824519E067-33489
chr1182824756182824854E067-33154
chr1182812593182812642E068-45366
chr1182814736182814780E068-43228
chr1182859218182859480E0681210
chr1182859484182859583E0681476
chr1182813060182813114E069-44894
chr1182813476182813516E069-44492
chr1182814736182814780E069-43228
chr1182815161182815267E069-42741
chr1182812593182812642E070-45366
chr1182812701182812741E070-45267
chr1182813060182813114E070-44894
chr1182813476182813516E070-44492
chr1182814736182814780E070-43228
chr1182812593182812642E071-45366
chr1182814736182814780E071-43228
chr1182815161182815267E071-42741
chr1182812593182812642E072-45366
chr1182812701182812741E072-45267
chr1182813060182813114E072-44894
chr1182813476182813516E072-44492
chr1182814736182814780E072-43228
chr1182824756182824854E072-33154
chr1182814736182814780E073-43228
chr1182815161182815267E073-42741
chr1182824756182824854E073-33154
chr1182825134182825362E073-32646
chr1182814736182814780E074-43228
chr1182815161182815267E074-42741
chr1182859218182859480E0741210
chr1182859484182859583E0741476
chr1182813060182813114E082-44894
chr1182813476182813516E082-44492
chr1182895292182895573E08237284









Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1182809689182809756E067-48252
chr1182809837182810000E067-48008
chr1182809689182809756E068-48252
chr1182809837182810000E068-48008
chr1182809689182809756E069-48252
chr1182809837182810000E069-48008
chr1182809689182809756E070-48252
chr1182809837182810000E070-48008
chr1182809689182809756E071-48252
chr1182809837182810000E071-48008
chr1182809689182809756E072-48252
chr1182809837182810000E072-48008
chr1182809689182809756E073-48252
chr1182809837182810000E073-48008
chr1182809689182809756E074-48252
chr1182809837182810000E074-48008
chr1182809689182809756E081-48252
chr1182809837182810000E081-48008
chr1182809689182809756E082-48252
chr1182809837182810000E082-48008