rs4769281

Homo sapiens
A>G / A>T
LOC105370114 : Non Coding Transcript Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0421 (12611/29926,GnomAD)
G=0433 (12614/29116,TOPMED)
G=0392 (1961/5008,1000G)
G=0414 (1594/3854,ALSPAC)
G=0420 (1557/3708,TWINSUK)
chr13:23681651 (GRCh38.p7) (13q12.12)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.23681651A>G
GRCh38.p7 chr 13NC_000013.11:g.23681651A>T
GRCh37.p13 chr 13NC_000013.10:g.24255790A>G
GRCh37.p13 chr 13NC_000013.10:g.24255790A>T

Gene: LOC105370114, uncharacterized LOC105370114(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105370114 transcript variant X2XR_001749788.1:n....XR_001749788.1:n.221T>CT>CNon Coding Transcript Variant
LOC105370114 transcript variant X2XR_001749788.1:n....XR_001749788.1:n.221T>AT>ANon Coding Transcript Variant
LOC105370114 transcript variant X1XR_941748.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.570G=0.430
1000GenomesAmericanSub694A=0.560G=0.440
1000GenomesEast AsianSub1008A=0.718G=0.282
1000GenomesEuropeSub1006A=0.584G=0.416
1000GenomesGlobalStudy-wide5008A=0.608G=0.392
1000GenomesSouth AsianSub978A=0.600G=0.400
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.586G=0.414
The Genome Aggregation DatabaseAfricanSub8706A=0.558G=0.442
The Genome Aggregation DatabaseAmericanSub838A=0.600G=0.400
The Genome Aggregation DatabaseEast AsianSub1618A=0.711G=0.289
The Genome Aggregation DatabaseEuropeSub18462A=0.579G=0.420
The Genome Aggregation DatabaseGlobalStudy-wide29926A=0.578G=0.421
The Genome Aggregation DatabaseOtherSub302A=0.370G=0.630
Trans-Omics for Precision MedicineGlobalStudy-wide29116A=0.566G=0.433
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.580G=0.420
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs47692810.000611alcohol dependence21314694

eQTL of rs4769281 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 rs4769281 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.