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rs398122810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs398122810(-;-)
Make rs398122810(-;TG)
ReferenceGRCh38 38.1/141
Chromosome1
Position156861141
GeneNTRK1
is asnp
is mentioned by
dbSNPrs398122810
ebirs398122810
HLIrs398122810
Exacrs398122810
Varsomers398122810
Maprs398122810
PheGenIrs398122810
hapmaprs398122810
1000 genomesrs398122810
hgdprs398122810
ensemblrs398122810
gopubmedrs398122810
geneviewrs398122810
scholarrs398122810
googlers398122810
pharmgkbrs398122810
gwascentralrs398122810
openSNPrs398122810
23andMers398122810
23andMe allrs398122810
SNP Nexus

SNPshotrs398122810
SNPdbers398122810
MSV3drs398122810
GWAS Ctlgrs398122810
Max Magnitude0
ClinVar
Risk rs398122810(;)
Alt rs398122810(;)
Reference rs398122810(TG;TG)
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.156830933_156830934delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000022807.18,