rs1064794589

Orientation

plus

Stabilized

plus

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

Chromosome

19

Position

35032595

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs1064794589
dbSNP (classic)	rs1064794589
ClinGen	rs1064794589
ebi	rs1064794589
HLI	rs1064794589
Exac	rs1064794589
Gnomad	rs1064794589
Varsome	rs1064794589
LitVar	rs1064794589
Map	rs1064794589
PheGenI	rs1064794589
Biobank	rs1064794589
1000 genomes	rs1064794589
hgdp	rs1064794589
ensembl	rs1064794589
geneview	rs1064794589
scholar	rs1064794589
google	rs1064794589
pharmgkb	rs1064794589
gwascentral	rs1064794589
openSNP	rs1064794589
23andMe	rs1064794589
SNPshot	rs1064794589
SNPdbe	rs1064794589
MSV3d	rs1064794589
GWAS Ctlg	rs1064794589

Max Magnitude

0

ClinVar
Risk	rs1064794589(-;-)
Alt	rs1064794589(-;-)
Reference	Rs1064794589(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN1B
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.35523499delC
CLNSRC
CLNACC	RCV000480433.1,