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rs121964869

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Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964869(A;G)
Make rs121964869(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156873858
GeneNTRK1
is asnp
is mentioned by
dbSNPrs121964869
ebirs121964869
HLIrs121964869
Exacrs121964869
Varsomers121964869
Maprs121964869
PheGenIrs121964869
hapmaprs121964869
1000 genomesrs121964869
hgdprs121964869
ensemblrs121964869
gopubmedrs121964869
geneviewrs121964869
scholarrs121964869
googlers121964869
pharmgkbrs121964869
gwascentralrs121964869
openSNPrs121964869
23andMers121964869
23andMe allrs121964869
SNP Nexus

SNPshotrs121964869
SNPdbers121964869
MSV3drs121964869
GWAS Ctlgrs121964869
Max Magnitude0
OMIM191315
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121964869(G;G)
Alt rs121964869(G;G)
Reference rs121964869(A;A)
Significance Pathogenic
Disease Hereditary insensitivity to pain with anhidrosis
Variation info
Gene NTRK1
CLNDBN Hereditary insensitivity to pain with anhidrosis
Reversed 0
HGVS NC_000001.10:g.156843650A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013104.16,