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

rs786205837

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205837(A;A)
Make rs786205837(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position35032560
GeneSCN1B
is asnp
is mentioned by
dbSNPrs786205837
ebirs786205837
HLIrs786205837
Exacrs786205837
Varsomers786205837
Maprs786205837
PheGenIrs786205837
hapmaprs786205837
1000 genomesrs786205837
hgdprs786205837
ensemblrs786205837
gopubmedrs786205837
geneviewrs786205837
scholarrs786205837
googlers786205837
pharmgkbrs786205837
gwascentralrs786205837
openSNPrs786205837
23andMers786205837
23andMe allrs786205837
SNP Nexus

SNPshotrs786205837
SNPdbers786205837
MSV3drs786205837
GWAS Ctlgrs786205837
Max Magnitude0
ClinVar
Risk rs786205837(A;A)
Alt rs786205837(A;A)
Reference rs786205837(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1B
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.35523464G>A
CLNSRC
CLNACC RCV000171059.2,