rs540635787

Orientation

plus

Stabilized

plus

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

Make rs540635787(A;A)

Make rs540635787(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28694073

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs540635787
dbSNP (classic)	rs540635787
ClinGen	rs540635787
ebi	rs540635787
HLI	rs540635787
Exac	rs540635787
Gnomad	rs540635787
Varsome	rs540635787
LitVar	rs540635787
Map	rs540635787
PheGenI	rs540635787
Biobank	rs540635787
1000 genomes	rs540635787
hgdp	rs540635787
ensembl	rs540635787
geneview	rs540635787
scholar	rs540635787
google	rs540635787
pharmgkb	rs540635787
gwascentral	rs540635787
openSNP	rs540635787
23andMe	rs540635787
SNPshot	rs540635787
SNPdbe	rs540635787
MSV3d	rs540635787
GWAS Ctlg	rs540635787

Max Magnitude

0

ClinVar
Risk	rs540635787(A;A) rs540635787(C;C) rs540635787(T;T)
Alt	rs540635787(A;A) rs540635787(C;C) rs540635787(T;T)
Reference	Rs540635787(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Carcinoma of colon Lung cancer Malignant tumor of prostate
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not specified Carcinoma of colon Lung cancer Malignant tumor of prostate
Reversed	0
HGVS	NC_000022.10:g.29090061G>A; NC_000022.10:g.29090061G>C; NC_000022.10:g.29090061G>T
CLNSRC
CLNACC	RCV000115999.6, RCV000206044.3, RCV000212462.2, RCV000234795.1, RCV000476206.1, RCV000213121.1, RCV000219946.1, RCV000470899.1,