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rs141686175

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs141686175(A;G)
Make rs141686175(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38872215
GeneSCN11A
is asnp
is mentioned by
dbSNPrs141686175
ebirs141686175
HLIrs141686175
Exacrs141686175
Varsomers141686175
Maprs141686175
PheGenIrs141686175
hapmaprs141686175
1000 genomesrs141686175
hgdprs141686175
ensemblrs141686175
gopubmedrs141686175
geneviewrs141686175
scholarrs141686175
googlers141686175
pharmgkbrs141686175
gwascentralrs141686175
openSNPrs141686175
23andMers141686175
23andMe allrs141686175
SNP Nexus

SNPshotrs141686175
SNPdbers141686175
MSV3drs141686175
GWAS Ctlgrs141686175
Max Magnitude0
ClinVar
Risk rs141686175(G;G)
Alt rs141686175(G;G)
Reference rs141686175(A;A)
Significance Pathogenic
Disease Episodic pain syndrome
Variation info
Gene SCN11A
CLNDBN Episodic pain syndrome, familial, 3
Reversed 0
HGVS NC_000003.11:g.38913706A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144934.3,