rs587781705

Orientation

minus

Stabilized

minus

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

Make rs587781705(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

28734506

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs587781705
dbSNP (classic)	rs587781705
ClinGen	rs587781705
ebi	rs587781705
HLI	rs587781705
Exac	rs587781705
Gnomad	rs587781705
Varsome	rs587781705
LitVar	rs587781705
Map	rs587781705
PheGenI	rs587781705
Biobank	rs587781705
1000 genomes	rs587781705
hgdp	rs587781705
ensembl	rs587781705
geneview	rs587781705
scholar	rs587781705
google	rs587781705
pharmgkb	rs587781705
gwascentral	rs587781705
openSNP	rs587781705
23andMe	rs587781705
SNPshot	rs587781705
SNPdbe	rs587781705
MSV3d	rs587781705
GWAS Ctlg	rs587781705

Max Magnitude

6

ClinVar
Risk	rs587781705(G;G)
Alt	rs587781705(G;G)
Reference	Rs587781705(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29130494A>C
CLNSRC
CLNACC	RCV000129876.3,