rs876658302

Orientation

minus

Stabilized

minus

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

Make rs876658302(-;-)

Make rs876658302(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28695772

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs876658302
dbSNP (classic)	rs876658302
ClinGen	rs876658302
ebi	rs876658302
HLI	rs876658302
Exac	rs876658302
Gnomad	rs876658302
Varsome	rs876658302
LitVar	rs876658302
Map	rs876658302
PheGenI	rs876658302
Biobank	rs876658302
1000 genomes	rs876658302
hgdp	rs876658302
ensembl	rs876658302
geneview	rs876658302
scholar	rs876658302
google	rs876658302
pharmgkb	rs876658302
gwascentral	rs876658302
openSNP	rs876658302
23andMe	rs876658302
SNPshot	rs876658302
SNPdbe	rs876658302
MSV3d	rs876658302
GWAS Ctlg	rs876658302

Max Magnitude

0

ClinVar
Risk	rs876658302(-;-)
Alt	rs876658302(-;-)
Reference	Rs876658302(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29091760delA
CLNSRC
CLNACC	RCV000223384.1,