rs9523810

Homo sapiens
A>C
LINC00430 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
C=0077 (2315/29968,GnomAD)
C=0084 (2451/29118,TOPMED)
C=0068 (342/5008,1000G)
C=0104 (401/3854,ALSPAC)
C=0101 (374/3708,TWINSUK)
chr13:86914128 (GRCh38.p7) (13q31.1)
AD
GWASdb2
1   publication(s)
See rs on genome
2 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.86914128A>C
GRCh37.p13 chr 13NC_000013.10:g.87566383A>C

Gene: LINC00430, long intergenic non-protein coding RNA 430(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LINC00430 transcriptNR_132371.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.943C=0.057
1000GenomesAmericanSub694A=0.940C=0.060
1000GenomesEast AsianSub1008A=0.965C=0.035
1000GenomesEuropeSub1006A=0.908C=0.092
1000GenomesGlobalStudy-wide5008A=0.932C=0.068
1000GenomesSouth AsianSub978A=0.900C=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.896C=0.104
The Genome Aggregation DatabaseAfricanSub8728A=0.935C=0.065
The Genome Aggregation DatabaseAmericanSub838A=0.950C=0.050
The Genome Aggregation DatabaseEast AsianSub1620A=0.951C=0.049
The Genome Aggregation DatabaseEuropeSub18480A=0.914C=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29968A=0.922C=0.077
The Genome Aggregation DatabaseOtherSub302A=0.850C=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.915C=0.084
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.899C=0.101
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs95238100.000197alcohol consumption23743675

eQTL of rs9523810 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87566383SLITRK5ENSG00000165300.6A>C7.2166e-3-758487Cerebellar_Hemisphere

meQTL of rs9523810 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 )
chr138752272887523350E081-43033
chr138757943087579480E08113047