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rs121964870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964870(A;G)
Make rs121964870(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156876526
GeneNTRK1
is asnp
is mentioned by
dbSNPrs121964870
ebirs121964870
HLIrs121964870
Exacrs121964870
Varsomers121964870
Maprs121964870
PheGenIrs121964870
hapmaprs121964870
1000 genomesrs121964870
hgdprs121964870
ensemblrs121964870
gopubmedrs121964870
geneviewrs121964870
scholarrs121964870
googlers121964870
pharmgkbrs121964870
gwascentralrs121964870
openSNPrs121964870
23andMers121964870
23andMe allrs121964870
SNP Nexus

SNPshotrs121964870
SNPdbers121964870
MSV3drs121964870
GWAS Ctlgrs121964870
Max Magnitude0
OMIM191315
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121964870(G;G)
Alt rs121964870(G;G)
Reference rs121964870(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.156846318A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013105.18,