rs786205792

Orientation

minus

Stabilized

minus

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

Make rs786205792(C;C)

Make rs786205792(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

115701359

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs786205792
dbSNP (classic)	rs786205792
ClinGen	rs786205792
ebi	rs786205792
HLI	rs786205792
Exac	rs786205792
Gnomad	rs786205792
Varsome	rs786205792
LitVar	rs786205792
Map	rs786205792
PheGenI	rs786205792
Biobank	rs786205792
1000 genomes	rs786205792
hgdp	rs786205792
ensembl	rs786205792
geneview	rs786205792
scholar	rs786205792
google	rs786205792
pharmgkb	rs786205792
gwascentral	rs786205792
openSNP	rs786205792
23andMe	rs786205792
SNPshot	rs786205792
SNPdbe	rs786205792
MSV3d	rs786205792
GWAS Ctlg	rs786205792

Max Magnitude

0

ClinVar
Risk	rs786205792(C;C)
Alt	rs786205792(C;C)
Reference	Rs786205792(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CASQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.116243980C>G
CLNSRC
CLNACC	RCV000170896.3,