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rs121908911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908911(A;A)
Make rs121908911(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166228971
GeneAC010127.3, SCN9A
is asnp
is mentioned by
dbSNPrs121908911
ebirs121908911
HLIrs121908911
Exacrs121908911
Varsomers121908911
Maprs121908911
PheGenIrs121908911
hapmaprs121908911
1000 genomesrs121908911
hgdprs121908911
ensemblrs121908911
gopubmedrs121908911
geneviewrs121908911
scholarrs121908911
googlers121908911
pharmgkbrs121908911
gwascentralrs121908911
openSNPrs121908911
23andMers121908911
23andMe allrs121908911
SNP Nexus

SNPshotrs121908911
SNPdbers121908911
MSV3drs121908911
GWAS Ctlgrs121908911
Max Magnitude0
OMIM603415
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908911(A;A)
Alt rs121908911(A;A)
Reference rs121908911(T;T)
Significance Pathogenic
Disease Paroxysmal extreme pain disorder
Variation info
Gene LOC101929680 SCN9A
CLNDBN Paroxysmal extreme pain disorder
Reversed 1
HGVS NC_000002.11:g.167085481A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006729.2,