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rs606231467

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231467(A;A)
Make rs606231467(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156876128
GeneNTRK1
is asnp
is mentioned by
dbSNPrs606231467
ebirs606231467
HLIrs606231467
Exacrs606231467
Varsomers606231467
Maprs606231467
PheGenIrs606231467
hapmaprs606231467
1000 genomesrs606231467
hgdprs606231467
ensemblrs606231467
gopubmedrs606231467
geneviewrs606231467
scholarrs606231467
googlers606231467
pharmgkbrs606231467
gwascentralrs606231467
openSNPrs606231467
23andMers606231467
23andMe allrs606231467
SNP Nexus

SNPshotrs606231467
SNPdbers606231467
MSV3drs606231467
GWAS Ctlgrs606231467
Max Magnitude0
ClinVar
Risk rs606231467(A;A)
Alt rs606231467(A;A)
Reference rs606231467(G;G)
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.156845920G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148946.3,