rs757789935

Orientation

plus

Stabilized

plus

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

Make rs757789935(A;G)

Make rs757789935(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

115768306

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs757789935
dbSNP (classic)	rs757789935
ClinGen	rs757789935
ebi	rs757789935
HLI	rs757789935
Exac	rs757789935
Gnomad	rs757789935
Varsome	rs757789935
LitVar	rs757789935
Map	rs757789935
PheGenI	rs757789935
Biobank	rs757789935
1000 genomes	rs757789935
hgdp	rs757789935
ensembl	rs757789935
geneview	rs757789935
scholar	rs757789935
google	rs757789935
pharmgkb	rs757789935
gwascentral	rs757789935
openSNP	rs757789935
23andMe	rs757789935
SNPshot	rs757789935
SNPdbe	rs757789935
MSV3d	rs757789935
GWAS Ctlg	rs757789935

Max Magnitude

0

ClinVar
Risk	rs757789935(G;G)
Alt	rs757789935(G;G)
Reference	Rs757789935(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CASQ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.116310927A>G
CLNSRC
CLNACC	RCV000489910.1,