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rs606231280

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231280(C;C)
Make rs606231280(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38909154
GeneSCN11A
is asnp
is mentioned by
dbSNPrs606231280
ebirs606231280
HLIrs606231280
Exacrs606231280
Varsomers606231280
Maprs606231280
PheGenIrs606231280
hapmaprs606231280
1000 genomesrs606231280
hgdprs606231280
ensemblrs606231280
gopubmedrs606231280
geneviewrs606231280
scholarrs606231280
googlers606231280
pharmgkbrs606231280
gwascentralrs606231280
openSNPrs606231280
23andMers606231280
23andMe allrs606231280
SNP Nexus

SNPshotrs606231280
SNPdbers606231280
MSV3drs606231280
GWAS Ctlgrs606231280
Max Magnitude0
ClinVar
Risk rs606231280(C;C)
Alt rs606231280(C;C)
Reference rs606231280(T;T)
Significance Pathogenic
Disease Episodic pain syndrome
Variation info
Gene SCN11A
CLNDBN Episodic pain syndrome, familial, 3
Reversed 1
HGVS NC_000003.11:g.38950645A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144935.3,