rs876659519

Orientation

minus

Stabilized

minus

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

Make rs876659519(G;G)

Make rs876659519(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28703519

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs876659519
dbSNP (classic)	rs876659519
ClinGen	rs876659519
ebi	rs876659519
HLI	rs876659519
Exac	rs876659519
Gnomad	rs876659519
Varsome	rs876659519
LitVar	rs876659519
Map	rs876659519
PheGenI	rs876659519
Biobank	rs876659519
1000 genomes	rs876659519
hgdp	rs876659519
ensembl	rs876659519
geneview	rs876659519
scholar	rs876659519
google	rs876659519
pharmgkb	rs876659519
gwascentral	rs876659519
openSNP	rs876659519
23andMe	rs876659519
SNPshot	rs876659519
SNPdbe	rs876659519
MSV3d	rs876659519
GWAS Ctlg	rs876659519

Max Magnitude

0

ClinVar
Risk	rs876659519(G;G)
Alt	rs876659519(G;G)
Reference	Rs876659519(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.29099507A>C
CLNSRC
CLNACC	RCV000215015.2,