Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852694(C;T)
Make rs137852694(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position36517739
GeneNKX2-1
is asnp
is mentioned by
dbSNPrs137852694
ebirs137852694
HLIrs137852694
Exacrs137852694
Varsomers137852694
Maprs137852694
PheGenIrs137852694
hapmaprs137852694
1000 genomesrs137852694
hgdprs137852694
ensemblrs137852694
gopubmedrs137852694
geneviewrs137852694
scholarrs137852694
googlers137852694
pharmgkbrs137852694
gwascentralrs137852694
openSNPrs137852694
23andMers137852694
23andMe allrs137852694
SNP Nexus

SNPshotrs137852694
SNPdbers137852694
MSV3drs137852694
GWAS Ctlgrs137852694
Max Magnitude0
OMIM600635
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137852694(T;T)
Alt rs137852694(T;T)
Reference rs137852694(C;C)
Significance Pathogenic
Disease Benign hereditary chorea
Variation info
Gene NKX2-1-AS1 NKX2-1
CLNDBN Benign hereditary chorea
Reversed 1
HGVS NC_000014.8:g.36986944G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009543.5,