rs545982789

Orientation

plus

Stabilized

plus

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

Make rs545982789(A;G)

Make rs545982789(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28711907

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs545982789
dbSNP (classic)	rs545982789
ClinGen	rs545982789
ebi	rs545982789
HLI	rs545982789
Exac	rs545982789
Gnomad	rs545982789
Varsome	rs545982789
LitVar	rs545982789
Map	rs545982789
PheGenI	rs545982789
Biobank	rs545982789
1000 genomes	rs545982789
hgdp	rs545982789
ensembl	rs545982789
geneview	rs545982789
scholar	rs545982789
google	rs545982789
pharmgkb	rs545982789
gwascentral	rs545982789
openSNP	rs545982789
23andMe	rs545982789
SNPshot	rs545982789
SNPdbe	rs545982789
MSV3d	rs545982789
GWAS Ctlg	rs545982789

Max Magnitude

0

ClinVar
Risk	rs545982789(G;G)
Alt	rs545982789(G;G)
Reference	Rs545982789(A;A)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	CHEK2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000022.10:g.29107895A>G
CLNSRC
CLNACC	RCV000205137.1,