rs794728788

Orientation

plus

Stabilized

plus

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

Make rs794728788(A;C)

Make rs794728788(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

237784257

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs794728788
dbSNP (classic)	rs794728788
ClinGen	rs794728788
ebi	rs794728788
HLI	rs794728788
Exac	rs794728788
Gnomad	rs794728788
Varsome	rs794728788
LitVar	rs794728788
Map	rs794728788
PheGenI	rs794728788
Biobank	rs794728788
1000 genomes	rs794728788
hgdp	rs794728788
ensembl	rs794728788
geneview	rs794728788
scholar	rs794728788
google	rs794728788
pharmgkb	rs794728788
gwascentral	rs794728788
openSNP	rs794728788
23andMe	rs794728788
SNPshot	rs794728788
SNPdbe	rs794728788
MSV3d	rs794728788
GWAS Ctlg	rs794728788

Max Magnitude

0

ClinVar
Risk	rs794728788(C;C)
Alt	rs794728788(C;C)
Reference	Rs794728788(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RYR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.237947557A>C
CLNSRC
CLNACC	RCV000182822.1,