rs587780170

Orientation

minus

Stabilized

minus

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

Make rs587780170(C;C)

Make rs587780170(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

28695786

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs587780170
dbSNP (classic)	rs587780170
ClinGen	rs587780170
ebi	rs587780170
HLI	rs587780170
Exac	rs587780170
Gnomad	rs587780170
Varsome	rs587780170
LitVar	rs587780170
Map	rs587780170
PheGenI	rs587780170
Biobank	rs587780170
1000 genomes	rs587780170
hgdp	rs587780170
ensembl	rs587780170
geneview	rs587780170
scholar	rs587780170
google	rs587780170
pharmgkb	rs587780170
gwascentral	rs587780170
openSNP	rs587780170
23andMe	rs587780170
SNPshot	rs587780170
SNPdbe	rs587780170
MSV3d	rs587780170
GWAS Ctlg	rs587780170

Max Magnitude

0

ClinVar
Risk	rs587780170(A;A) rs587780170(C;C) rs587780170(T;T)
Alt	rs587780170(A;A) rs587780170(C;C) rs587780170(T;T)
Reference	Rs587780170(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Variation	info
Gene	CHEK2
CLNDBN	Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast
Reversed	1
HGVS	NC_000022.10:g.29091774C>A; NC_000022.10:g.29091774C>G; NC_000022.10:g.29091774C>T
CLNSRC
CLNACC	RCV000422650.1, RCV000115987.6, RCV000212454.2, RCV000230538.2, RCV000467802.1,