rs876660801

Orientation

minus

Stabilized

minus

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

Make rs876660801(-;-)

Make rs876660801(-;GT)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28695125

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs876660801
dbSNP (classic)	rs876660801
ClinGen	rs876660801
ebi	rs876660801
HLI	rs876660801
Exac	rs876660801
Gnomad	rs876660801
Varsome	rs876660801
LitVar	rs876660801
Map	rs876660801
PheGenI	rs876660801
Biobank	rs876660801
1000 genomes	rs876660801
hgdp	rs876660801
ensembl	rs876660801
geneview	rs876660801
scholar	rs876660801
google	rs876660801
pharmgkb	rs876660801
gwascentral	rs876660801
openSNP	rs876660801
23andMe	rs876660801
SNPshot	rs876660801
SNPdbe	rs876660801
MSV3d	rs876660801
GWAS Ctlg	rs876660801

Max Magnitude

0

ClinVar
Risk	rs876660801(-;-)
Alt	rs876660801(-;-)
Reference	Rs876660801(GT;GT)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29091113_29091114delAC
CLNSRC
CLNACC	RCV000220512.1,