rs12094153

Homo sapiens
G>A
TNN : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0367 (10968/29866,GnomAD)
A=0319 (9315/29118,TOPMED)
A=0256 (1282/5008,1000G)
A=0418 (1612/3854,ALSPAC)
A=0452 (1676/3708,TWINSUK)
chr1:175124889 (GRCh38.p7) (1q25.1)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.175124889G>A
GRCh37.p13 chr 1NC_000001.10:g.175094025G>A

Gene: TNN, tenascin N(plus strand)

Molecule type Change Amino acid[Codon] SO Term
TNN transcriptNM_022093.1:c.N/AIntron Variant
TNN transcript variant X1XM_017002048.1:c.N/AIntron Variant
TNN transcript variant X2XM_017002049.1:c.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.724A=0.276
1000GenomesAmericanSub694G=0.730A=0.270
1000GenomesEast AsianSub1008G=0.903A=0.097
1000GenomesEuropeSub1006G=0.562A=0.438
1000GenomesGlobalStudy-wide5008G=0.744A=0.256
1000GenomesSouth AsianSub978G=0.810A=0.190
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.582A=0.418
The Genome Aggregation DatabaseAfricanSub8678G=0.724A=0.276
The Genome Aggregation DatabaseAmericanSub836G=0.760A=0.240
The Genome Aggregation DatabaseEast AsianSub1610G=0.912A=0.088
The Genome Aggregation DatabaseEuropeSub18442G=0.558A=0.441
The Genome Aggregation DatabaseGlobalStudy-wide29866G=0.632A=0.367
The Genome Aggregation DatabaseOtherSub300G=0.700A=0.300
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.680A=0.319
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.548A=0.452
PMID Title Author Journal
21703634A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.Wang KSJ Psychiatr Res
21956439Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.Zuo LNeuropsychopharmacology

P-Value

SNP ID p-value Traits Study
rs120941535.49E-05alcohol dependence21703634

eQTL of rs12094153 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 rs12094153 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 )
chr1175127262175127638E06733237
chr1175127726175127793E06733701
chr1175121212175121706E06927187
chr1175138495175138718E06944470
chr1175117508175117593E07023483
chr1175131566175131616E07037541
chr1175131702175131793E07037677
chr1175131845175132044E07037820
chr1175132208175132358E07038183
chr1175121212175121706E07227187
chr1175115170175115364E08121145
chr1175115429175115500E08121404
chr1175115737175116333E08121712
chr1175116438175116534E08122413
chr1175116763175117071E08122738
chr1175117325175117401E08123300
chr1175117508175117593E08123483
chr1175120951175121040E08126926
chr1175121212175121706E08127187
chr1175127262175127638E08233237
chr1175127726175127793E08233701