rs587780185

Orientation

minus

Stabilized

minus

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

Make rs587780185(A;G)

Make rs587780185(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28725004

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs587780185
dbSNP (classic)	rs587780185
ClinGen	rs587780185
ebi	rs587780185
HLI	rs587780185
Exac	rs587780185
Gnomad	rs587780185
Varsome	rs587780185
LitVar	rs587780185
Map	rs587780185
PheGenI	rs587780185
Biobank	rs587780185
1000 genomes	rs587780185
hgdp	rs587780185
ensembl	rs587780185
geneview	rs587780185
scholar	rs587780185
google	rs587780185
pharmgkb	rs587780185
gwascentral	rs587780185
openSNP	rs587780185
23andMe	rs587780185
SNPshot	rs587780185
SNPdbe	rs587780185
MSV3d	rs587780185
GWAS Ctlg	rs587780185

Max Magnitude

0

Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312]

ClinVar
Risk	rs587780185(G;G)
Alt	rs587780185(G;G)
Reference	Rs587780185(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000022.10:g.29120992T>C
CLNSRC
CLNACC	RCV000116026.7, RCV000212429.1, RCV000230801.2,