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

rs786205830

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205830(C;T)
Make rs786205830(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position35033544
GeneSCN1B
is asnp
is mentioned by
dbSNPrs786205830
ebirs786205830
HLIrs786205830
Exacrs786205830
Varsomers786205830
Maprs786205830
PheGenIrs786205830
hapmaprs786205830
1000 genomesrs786205830
hgdprs786205830
ensemblrs786205830
gopubmedrs786205830
geneviewrs786205830
scholarrs786205830
googlers786205830
pharmgkbrs786205830
gwascentralrs786205830
openSNPrs786205830
23andMers786205830
23andMe allrs786205830
SNP Nexus

SNPshotrs786205830
SNPdbers786205830
MSV3drs786205830
GWAS Ctlgrs786205830
Max Magnitude0
ClinVar
Risk rs786205830(T;T)
Alt rs786205830(T;T)
Reference rs786205830(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1B
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.35524448C>T
CLNSRC
CLNACC RCV000171038.3,