rs1060502698

Orientation

minus

Stabilized

minus

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

Make rs1060502698(A;A)

Make rs1060502698(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

28689216

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs1060502698
dbSNP (classic)	rs1060502698
ClinGen	rs1060502698
ebi	rs1060502698
HLI	rs1060502698
Exac	rs1060502698
Gnomad	rs1060502698
Varsome	rs1060502698
LitVar	rs1060502698
Map	rs1060502698
PheGenI	rs1060502698
Biobank	rs1060502698
1000 genomes	rs1060502698
hgdp	rs1060502698
ensembl	rs1060502698
geneview	rs1060502698
scholar	rs1060502698
google	rs1060502698
pharmgkb	rs1060502698
gwascentral	rs1060502698
openSNP	rs1060502698
23andMe	rs1060502698
SNPshot	rs1060502698
SNPdbe	rs1060502698
MSV3d	rs1060502698
GWAS Ctlg	rs1060502698

Max Magnitude

0

ClinVar
Risk	rs1060502698(A;A)
Alt	rs1060502698(A;A)
Reference	Rs1060502698(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.29085204C>T
CLNSRC
CLNACC	RCV000474737.1,