rs786205838

Orientation

plus

Stabilized

plus

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

Make rs786205838(A;G)

Make rs786205838(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

35032569

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs786205838
dbSNP (classic)	rs786205838
ClinGen	rs786205838
ebi	rs786205838
HLI	rs786205838
Exac	rs786205838
Gnomad	rs786205838
Varsome	rs786205838
LitVar	rs786205838
Map	rs786205838
PheGenI	rs786205838
Biobank	rs786205838
1000 genomes	rs786205838
hgdp	rs786205838
ensembl	rs786205838
geneview	rs786205838
scholar	rs786205838
google	rs786205838
pharmgkb	rs786205838
gwascentral	rs786205838
openSNP	rs786205838
23andMe	rs786205838
SNPshot	rs786205838
SNPdbe	rs786205838
MSV3d	rs786205838
GWAS Ctlg	rs786205838

Max Magnitude

0

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,