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rs794729216

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729216(A;A)
Make rs794729216(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166277134
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs794729216
ebirs794729216
HLIrs794729216
Exacrs794729216
Varsomers794729216
Maprs794729216
PheGenIrs794729216
hapmaprs794729216
1000 genomesrs794729216
hgdprs794729216
ensemblrs794729216
gopubmedrs794729216
geneviewrs794729216
scholarrs794729216
googlers794729216
pharmgkbrs794729216
gwascentralrs794729216
openSNPrs794729216
23andMers794729216
23andMe allrs794729216
SNP Nexus

SNPshotrs794729216
SNPdbers794729216
MSV3drs794729216
GWAS Ctlgrs794729216
Max Magnitude0
ClinVar
Risk rs794729216(A;A)
Alt rs794729216(A;A)
Reference rs794729216(G;G)
Significance Pathogenic
Disease Indifference to pain
Variation info
Gene LOC101929680 SCN9A
CLNDBN Indifference to pain, congenital, autosomal recessive
Reversed 1
HGVS NC_000002.11:g.167133644C>T
CLNSRC
CLNACC RCV000184036.1,