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rs797045060

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045060(C;C)
Make rs797045060(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156873822
GeneNTRK1
is asnp
is mentioned by
dbSNPrs797045060
ebirs797045060
HLIrs797045060
Exacrs797045060
Varsomers797045060
Maprs797045060
PheGenIrs797045060
hapmaprs797045060
1000 genomesrs797045060
hgdprs797045060
ensemblrs797045060
gopubmedrs797045060
geneviewrs797045060
scholarrs797045060
googlers797045060
pharmgkbrs797045060
gwascentralrs797045060
openSNPrs797045060
23andMers797045060
23andMe allrs797045060
SNP Nexus

SNPshotrs797045060
SNPdbers797045060
MSV3drs797045060
GWAS Ctlgrs797045060
Max Magnitude0
ClinVar
Risk rs797045060(C;C)
Alt rs797045060(C;C)
Reference rs797045060(G;G)
Significance Probable-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.156843614G>C
CLNSRC Baylor College of Medicine
CLNACC RCV000191114.1,