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rs121908913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908913(G;T)
Make rs121908913(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166228969
GeneAC010127.3, SCN9A
is asnp
is mentioned by
dbSNPrs121908913
ebirs121908913
HLIrs121908913
Exacrs121908913
Varsomers121908913
Maprs121908913
PheGenIrs121908913
hapmaprs121908913
1000 genomesrs121908913
hgdprs121908913
ensemblrs121908913
gopubmedrs121908913
geneviewrs121908913
scholarrs121908913
googlers121908913
pharmgkbrs121908913
gwascentralrs121908913
openSNPrs121908913
23andMers121908913
23andMe allrs121908913
SNP Nexus

SNPshotrs121908913
SNPdbers121908913
MSV3drs121908913
GWAS Ctlgrs121908913
Max Magnitude0
OMIM603415
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121908913(T;T)
Alt rs121908913(T;T)
Reference rs121908913(G;G)
Significance Pathogenic
Disease Paroxysmal extreme pain disorder
Variation info
Gene LOC101929680 SCN9A
CLNDBN Paroxysmal extreme pain disorder
Reversed 1
HGVS NC_000002.11:g.167085479C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006731.2,