rs786205791

Orientation

minus

Stabilized

minus

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

Make rs786205791(C;C)

Make rs786205791(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

115732900

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs786205791
dbSNP (classic)	rs786205791
ClinGen	rs786205791
ebi	rs786205791
HLI	rs786205791
Exac	rs786205791
Gnomad	rs786205791
Varsome	rs786205791
LitVar	rs786205791
Map	rs786205791
PheGenI	rs786205791
Biobank	rs786205791
1000 genomes	rs786205791
hgdp	rs786205791
ensembl	rs786205791
geneview	rs786205791
scholar	rs786205791
google	rs786205791
pharmgkb	rs786205791
gwascentral	rs786205791
openSNP	rs786205791
23andMe	rs786205791
SNPshot	rs786205791
SNPdbe	rs786205791
MSV3d	rs786205791
GWAS Ctlg	rs786205791

Max Magnitude

0

ClinVar
Risk	rs786205791(C;C)
Alt	rs786205791(C;C)
Reference	Rs786205791(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CASQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.116275521C>G
CLNSRC
CLNACC	RCV000170889.2,