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rs138404783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs138404783(A;G)
Make rs138404783(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38752313
GeneSCN10A
is asnp
is mentioned by
dbSNPrs138404783
ebirs138404783
HLIrs138404783
Exacrs138404783
Varsomers138404783
Maprs138404783
PheGenIrs138404783
hapmaprs138404783
1000 genomesrs138404783
hgdprs138404783
ensemblrs138404783
gopubmedrs138404783
geneviewrs138404783
scholarrs138404783
googlers138404783
pharmgkbrs138404783
gwascentralrs138404783
openSNPrs138404783
23andMers138404783
23andMe allrs138404783
SNP Nexus

SNPshotrs138404783
SNPdbers138404783
MSV3drs138404783
GWAS Ctlgrs138404783
Max Magnitude0
ClinVar
Risk rs138404783(G;G)
Alt rs138404783(G;G)
Reference rs138404783(A;A)
Significance Pathogenic
Disease Episodic pain syndrome
Variation info
Gene SCN10A
CLNDBN Episodic pain syndrome, familial, 2
Reversed 0
HGVS NC_000003.11:g.38793804A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000074497.4,