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rs606231466

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231466(A;T)
Make rs606231466(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156868651
GeneNTRK1
is asnp
is mentioned by
dbSNPrs606231466
ebirs606231466
HLIrs606231466
Exacrs606231466
Varsomers606231466
Maprs606231466
PheGenIrs606231466
hapmaprs606231466
1000 genomesrs606231466
hgdprs606231466
ensemblrs606231466
gopubmedrs606231466
geneviewrs606231466
scholarrs606231466
googlers606231466
pharmgkbrs606231466
gwascentralrs606231466
openSNPrs606231466
23andMers606231466
23andMe allrs606231466
SNP Nexus

SNPshotrs606231466
SNPdbers606231466
MSV3drs606231466
GWAS Ctlgrs606231466
Max Magnitude0
ClinVar
Risk rs606231466(T;T)
Alt rs606231466(T;T)
Reference Rs606231466(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.156838443A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000148945.5,