Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205838

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205838(A;G)
Make rs786205838(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position35032569
GeneSCN1B
is asnp
is mentioned by
dbSNPrs786205838
ebirs786205838
HLIrs786205838
Exacrs786205838
Varsomers786205838
Maprs786205838
PheGenIrs786205838
hapmaprs786205838
1000 genomesrs786205838
hgdprs786205838
ensemblrs786205838
gopubmedrs786205838
geneviewrs786205838
scholarrs786205838
googlers786205838
pharmgkbrs786205838
gwascentralrs786205838
openSNPrs786205838
23andMers786205838
23andMe allrs786205838
SNP Nexus

SNPshotrs786205838
SNPdbers786205838
MSV3drs786205838
GWAS Ctlgrs786205838
Max Magnitude0
ClinVar
Risk rs786205838(G;G)
Alt rs786205838(G;G)
Reference rs786205838(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SCN1B
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.35523473A>G
CLNSRC
CLNACC RCV000171060.3,