rs762381137

Orientation

plus

Stabilized

plus

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

Make rs762381137(A;G)

Make rs762381137(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

115717869

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs762381137
dbSNP (classic)	rs762381137
ClinGen	rs762381137
ebi	rs762381137
HLI	rs762381137
Exac	rs762381137
Gnomad	rs762381137
Varsome	rs762381137
LitVar	rs762381137
Map	rs762381137
PheGenI	rs762381137
Biobank	rs762381137
1000 genomes	rs762381137
hgdp	rs762381137
ensembl	rs762381137
geneview	rs762381137
scholar	rs762381137
google	rs762381137
pharmgkb	rs762381137
gwascentral	rs762381137
openSNP	rs762381137
23andMe	rs762381137
SNPshot	rs762381137
SNPdbe	rs762381137
MSV3d	rs762381137
GWAS Ctlg	rs762381137

Max Magnitude

0

ClinVar
Risk	rs762381137(G;G)
Alt	rs762381137(G;G)
Reference	Rs762381137(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CASQ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.116260490A>G
CLNSRC
CLNACC	RCV000170892.2,