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rs387906404

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906404(-;-)
Make rs387906404(-;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position36517576
GeneNKX2-1, NKX2-1-AS1
is asnp
is mentioned by
dbSNPrs387906404
ebirs387906404
HLIrs387906404
Exacrs387906404
Varsomers387906404
Maprs387906404
PheGenIrs387906404
hapmaprs387906404
1000 genomesrs387906404
hgdprs387906404
ensemblrs387906404
gopubmedrs387906404
geneviewrs387906404
scholarrs387906404
googlers387906404
pharmgkbrs387906404
gwascentralrs387906404
openSNPrs387906404
23andMers387906404
23andMe allrs387906404
SNP Nexus

SNPshotrs387906404
SNPdbers387906404
MSV3drs387906404
GWAS Ctlgrs387906404
Max Magnitude0
ClinVar
Risk rs387906404(;)
Alt rs387906404(;)
Reference rs387906404(G;G)
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.36986781delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009538.5,