rs587781699

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6	Breast cancer associated mutation
(C;G)	6	Breast cancer associated mutation
(G;G)	0	common in clinvar

Make rs587781699(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

28703504

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs587781699
dbSNP (classic)	rs587781699
ClinGen	rs587781699
ebi	rs587781699
HLI	rs587781699
Exac	rs587781699
Gnomad	rs587781699
Varsome	rs587781699
LitVar	rs587781699
Map	rs587781699
PheGenI	rs587781699
Biobank	rs587781699
1000 genomes	rs587781699
hgdp	rs587781699
ensembl	rs587781699
geneview	rs587781699
scholar	rs587781699
google	rs587781699
pharmgkb	rs587781699
gwascentral	rs587781699
openSNP	rs587781699
23andMe	rs587781699
SNPshot	rs587781699
SNPdbe	rs587781699
MSV3d	rs587781699
GWAS Ctlg	rs587781699

Max Magnitude

6

ClinVar
Risk	rs587781699(A;A) rs587781699(T;T)
Alt	rs587781699(A;A) rs587781699(T;T)
Reference	Rs587781699(G;G)
Significance	Probable-Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29099492C>A; NC_000022.10:g.29099492C>T
CLNSRC
CLNACC	RCV000219083.1, RCV000129866.2,