rs854061

Homo sapiens
G>A / G>C
LOC105375409 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0097 (2908/29980,GnomAD)
G==0097 (2837/29118,TOPMED)
G==0148 (743/5008,1000G)
chr7:95676056 (GRCh38.p7) (7q21.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.95676056G>A
GRCh38.p7 chr 7NC_000007.14:g.95676056G>C
GRCh37.p13 chr 7NC_000007.13:g.95305368G>A
GRCh37.p13 chr 7NC_000007.13:g.95305368G>C

Gene: LOC105375409, uncharacterized LOC105375409(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105375409 transcript variant X2XR_927773.2:n.N/AIntron Variant
LOC105375409 transcript variant X2XR_927774.2:n.N/AIntron Variant
LOC105375409 transcript variant X1XR_927772.2:n.N/AGenic Downstream Transcript Variant
LOC105375409 transcript variant X4XR_927775.2:n.N/AGenic Downstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.040A=0.960
1000GenomesAmericanSub694G=0.210A=0.790
1000GenomesEast AsianSub1008G=0.264A=0.736
1000GenomesEuropeSub1006G=0.119A=0.881
1000GenomesGlobalStudy-wide5008G=0.148A=0.852
1000GenomesSouth AsianSub978G=0.160A=0.840
The Genome Aggregation DatabaseAfricanSub8726G=0.052A=0.948
The Genome Aggregation DatabaseAmericanSub838G=0.190A=0.810
The Genome Aggregation DatabaseEast AsianSub1618G=0.221A=0.779
The Genome Aggregation DatabaseEuropeSub18496G=0.103A=0.896
The Genome Aggregation DatabaseGlobalStudy-wide29980G=0.097A=0.903
The Genome Aggregation DatabaseOtherSub302G=0.090A=0.910
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.097A=0.902
PMID Title Author Journal
21703634A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.Wang KSJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs8540617.22E-05alcohol dependence21703634

eQTL of rs854061 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 rs854061 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.