rs1060502716

Orientation

minus

Stabilized

minus

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

Make rs1060502716(A;A)

Make rs1060502716(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

28695874

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs1060502716
dbSNP (classic)	rs1060502716
ClinGen	rs1060502716
ebi	rs1060502716
HLI	rs1060502716
Exac	rs1060502716
Gnomad	rs1060502716
Varsome	rs1060502716
LitVar	rs1060502716
Map	rs1060502716
PheGenI	rs1060502716
Biobank	rs1060502716
1000 genomes	rs1060502716
hgdp	rs1060502716
ensembl	rs1060502716
geneview	rs1060502716
scholar	rs1060502716
google	rs1060502716
pharmgkb	rs1060502716
gwascentral	rs1060502716
openSNP	rs1060502716
23andMe	rs1060502716
SNPshot	rs1060502716
SNPdbe	rs1060502716
MSV3d	rs1060502716
GWAS Ctlg	rs1060502716

Max Magnitude

0

ClinVar
Risk	rs1060502716(A;A)
Alt	rs1060502716(A;A)
Reference	Rs1060502716(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	CHEK2
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000022.10:g.29091862C>T
CLNSRC
CLNACC	RCV000464247.1,