rs7741833

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
A==0443 (13263/29894,GnomAD)
A==0443 (12923/29118,TOPMED)
A==0454 (2275/5008,1000G)
A==0408 (1571/3854,ALSPAC)
A==0389 (1442/3708,TWINSUK)
chr6:120679901 (GRCh38.p7) (6q22.31)
AD
GWASdb2
1   publication(s)
See rs on genome
1 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.120679901A>G
GRCh37.p13 chr 6NC_000006.11:g.121001047A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.510G=0.490
1000GenomesAmericanSub694A=0.430G=0.570
1000GenomesEast AsianSub1008A=0.475G=0.525
1000GenomesEuropeSub1006A=0.410G=0.590
1000GenomesGlobalStudy-wide5008A=0.454G=0.546
1000GenomesSouth AsianSub978A=0.420G=0.580
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.408G=0.592
The Genome Aggregation DatabaseAfricanSub8704A=0.482G=0.518
The Genome Aggregation DatabaseAmericanSub838A=0.380G=0.620
The Genome Aggregation DatabaseEast AsianSub1614A=0.453G=0.547
The Genome Aggregation DatabaseEuropeSub18436A=0.427G=0.572
The Genome Aggregation DatabaseGlobalStudy-wide29894A=0.443G=0.556
The Genome Aggregation DatabaseOtherSub302A=0.420G=0.580
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.443G=0.556
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.389G=0.611
PMID Title Author Journal

P-Value

SNP ID p-value Traits Study
rs77418336.61E-06alcohol consumptionpha001397

eQTL of rs7741833 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 rs7741833 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 )
chr6120967829120968204E081-32843