rs786205837

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs786205837(A;A)

Make rs786205837(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

35032560

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs786205837
dbSNP (classic)	rs786205837
ClinGen	rs786205837
ebi	rs786205837
HLI	rs786205837
Exac	rs786205837
Gnomad	rs786205837
Varsome	rs786205837
LitVar	rs786205837
Map	rs786205837
PheGenI	rs786205837
Biobank	rs786205837
1000 genomes	rs786205837
hgdp	rs786205837
ensembl	rs786205837
geneview	rs786205837
scholar	rs786205837
google	rs786205837
pharmgkb	rs786205837
gwascentral	rs786205837
openSNP	rs786205837
23andMe	rs786205837
SNPshot	rs786205837
SNPdbe	rs786205837
MSV3d	rs786205837
GWAS Ctlg	rs786205837

Max Magnitude

0

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	UniProtKB (protein)
CLNACC	RCV000171059.2,