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rs121908914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908914(C;C)
Make rs121908914(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166204448
GeneAC010127.3, SCN9A
is asnp
is mentioned by
dbSNPrs121908914
ebirs121908914
HLIrs121908914
Exacrs121908914
Varsomers121908914
Maprs121908914
PheGenIrs121908914
hapmaprs121908914
1000 genomesrs121908914
hgdprs121908914
ensemblrs121908914
gopubmedrs121908914
geneviewrs121908914
scholarrs121908914
googlers121908914
pharmgkbrs121908914
gwascentralrs121908914
openSNPrs121908914
23andMers121908914
23andMe allrs121908914
SNP Nexus

SNPshotrs121908914
SNPdbers121908914
MSV3drs121908914
GWAS Ctlgrs121908914
Max Magnitude0
OMIM603415
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908914(C;C)
Alt rs121908914(C;C)
Reference rs121908914(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.167060958A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006732.2,