rs786205830

Orientation

plus

Stabilized

plus

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

Make rs786205830(C;T)

Make rs786205830(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

35033544

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs786205830
dbSNP (classic)	rs786205830
ClinGen	rs786205830
ebi	rs786205830
HLI	rs786205830
Exac	rs786205830
Gnomad	rs786205830
Varsome	rs786205830
LitVar	rs786205830
Map	rs786205830
PheGenI	rs786205830
Biobank	rs786205830
1000 genomes	rs786205830
hgdp	rs786205830
ensembl	rs786205830
geneview	rs786205830
scholar	rs786205830
google	rs786205830
pharmgkb	rs786205830
gwascentral	rs786205830
openSNP	rs786205830
23andMe	rs786205830
SNPshot	rs786205830
SNPdbe	rs786205830
MSV3d	rs786205830
GWAS Ctlg	rs786205830

Max Magnitude

0

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,