rs28909980

Orientation

minus

Stabilized

minus

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

Make rs28909980(A;A)

Make rs28909980(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28696957

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs28909980
dbSNP (classic)	rs28909980
ClinGen	rs28909980
ebi	rs28909980
HLI	rs28909980
Exac	rs28909980
Gnomad	rs28909980
Varsome	rs28909980
LitVar	rs28909980
Map	rs28909980
PheGenI	rs28909980
Biobank	rs28909980
1000 genomes	rs28909980
hgdp	rs28909980
ensembl	rs28909980
geneview	rs28909980
scholar	rs28909980
google	rs28909980
pharmgkb	rs28909980
gwascentral	rs28909980
openSNP	rs28909980
23andMe	rs28909980
SNPshot	rs28909980
SNPdbe	rs28909980
MSV3d	rs28909980
GWAS Ctlg	rs28909980

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs28909980(A;A)
Alt	rs28909980(A;A)
Reference	Rs28909980(G;G)
Significance	Probable-Pathogenic
Disease	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29092945C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000160431.3, RCV000205583.2, RCV000221549.1,