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rs267607030

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607030(A;G)
Make rs267607030(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position166311728
GeneSCN9A
is asnp
is mentioned by
dbSNPrs267607030
ebirs267607030
HLIrs267607030
Exacrs267607030
Varsomers267607030
Maprs267607030
PheGenIrs267607030
hapmaprs267607030
1000 genomesrs267607030
hgdprs267607030
ensemblrs267607030
gopubmedrs267607030
geneviewrs267607030
scholarrs267607030
googlers267607030
pharmgkbrs267607030
gwascentralrs267607030
openSNPrs267607030
23andMers267607030
23andMe allrs267607030
SNP Nexus

SNPshotrs267607030
SNPdbers267607030
MSV3drs267607030
GWAS Ctlgrs267607030
Max Magnitude0
ClinVar
Risk rs267607030(G;G)
Alt rs267607030(G;G)
Reference rs267607030(A;A)
Significance Pathogenic
Disease Primary erythromelalgia
Variation info
Gene SCN9A
CLNDBN Primary erythromelalgia
Reversed 1
HGVS NC_000002.11:g.167168238T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006742.2,