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rs200398202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200398202(C;G)
Make rs200398202(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position166284560
GeneSCN9A
is asnp
is mentioned by
dbSNPrs200398202
ebirs200398202
HLIrs200398202
Exacrs200398202
Varsomers200398202
Maprs200398202
PheGenIrs200398202
hapmaprs200398202
1000 genomesrs200398202
hgdprs200398202
ensemblrs200398202
gopubmedrs200398202
geneviewrs200398202
scholarrs200398202
googlers200398202
pharmgkbrs200398202
gwascentralrs200398202
openSNPrs200398202
23andMers200398202
23andMe allrs200398202
SNP Nexus

SNPshotrs200398202
SNPdbers200398202
MSV3drs200398202
GWAS Ctlgrs200398202
Max Magnitude0
ClinVar
Risk rs200398202(G,T;G,T)
Alt rs200398202(G,T;G,T)
Reference rs200398202(C;C)
Significance Pathogenic
Disease Small fiber neuropathy
Variation info
Gene LOC101929680 SCN9A
CLNDBN Small fiber neuropathy
Reversed 0
HGVS NC_000002.11:g.167141070C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023303.3,