rs876660862

Orientation

minus

Stabilized

minus

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

Make rs876660862(-;T)

Make rs876660862(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28703536

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs876660862
dbSNP (classic)	rs876660862
ClinGen	rs876660862
ebi	rs876660862
HLI	rs876660862
Exac	rs876660862
Gnomad	rs876660862
Varsome	rs876660862
LitVar	rs876660862
Map	rs876660862
PheGenI	rs876660862
Biobank	rs876660862
1000 genomes	rs876660862
hgdp	rs876660862
ensembl	rs876660862
geneview	rs876660862
scholar	rs876660862
google	rs876660862
pharmgkb	rs876660862
gwascentral	rs876660862
openSNP	rs876660862
23andMe	rs876660862
SNPshot	rs876660862
SNPdbe	rs876660862
MSV3d	rs876660862
GWAS Ctlg	rs876660862

Max Magnitude

0

ClinVar
Risk	rs876660862(T;T)
Alt	rs876660862(T;T)
Reference	Rs876660862(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29099525dupA
CLNSRC
CLNACC	RCV000213838.1,