rs761494650

Orientation

plus

Stabilized

plus

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

Make rs761494650(A;A)

Make rs761494650(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

28734637

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs761494650
dbSNP (classic)	rs761494650
ClinGen	rs761494650
ebi	rs761494650
HLI	rs761494650
Exac	rs761494650
Gnomad	rs761494650
Varsome	rs761494650
LitVar	rs761494650
Map	rs761494650
PheGenI	rs761494650
Biobank	rs761494650
1000 genomes	rs761494650
hgdp	rs761494650
ensembl	rs761494650
geneview	rs761494650
scholar	rs761494650
google	rs761494650
pharmgkb	rs761494650
gwascentral	rs761494650
openSNP	rs761494650
23andMe	rs761494650
SNPshot	rs761494650
SNPdbe	rs761494650
MSV3d	rs761494650
GWAS Ctlg	rs761494650

Max Magnitude

0

ClinVar
Risk	rs761494650(A;A)
Alt	rs761494650(A;A)
Reference	Rs761494650(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	0
HGVS	NC_000022.10:g.29130625G>A
CLNSRC	Inc.
CLNACC	RCV000167444.2, RCV000228262.2, RCV000485654.1,