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rs121908915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908915(C;T)
Make rs121908915(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166204439
GeneAC010127.3, SCN9A
is asnp
is mentioned by
dbSNPrs121908915
ebirs121908915
HLIrs121908915
Exacrs121908915
Varsomers121908915
Maprs121908915
PheGenIrs121908915
hapmaprs121908915
1000 genomesrs121908915
hgdprs121908915
ensemblrs121908915
gopubmedrs121908915
geneviewrs121908915
scholarrs121908915
googlers121908915
pharmgkbrs121908915
gwascentralrs121908915
openSNPrs121908915
23andMers121908915
23andMe allrs121908915
SNP Nexus

SNPshotrs121908915
SNPdbers121908915
MSV3drs121908915
GWAS Ctlgrs121908915
Max Magnitude0
OMIM603415
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908915(T;T)
Alt rs121908915(T;T)
Reference rs121908915(C;C)
Significance Pathogenic
Disease Paroxysmal extreme pain disorder
Variation info
Gene LOC101929680 SCN9A
CLNDBN Paroxysmal extreme pain disorder
Reversed 1
HGVS NC_000002.11:g.167060949G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006733.2,