rs753159426

Orientation

plus

Stabilized

plus

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

Make rs753159426(-;-)

Make rs753159426(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28695781

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs753159426
dbSNP (classic)	rs753159426
ClinGen	rs753159426
ebi	rs753159426
HLI	rs753159426
Exac	rs753159426
Gnomad	rs753159426
Varsome	rs753159426
LitVar	rs753159426
Map	rs753159426
PheGenI	rs753159426
Biobank	rs753159426
1000 genomes	rs753159426
hgdp	rs753159426
ensembl	rs753159426
geneview	rs753159426
scholar	rs753159426
google	rs753159426
pharmgkb	rs753159426
gwascentral	rs753159426
openSNP	rs753159426
23andMe	rs753159426
SNPshot	rs753159426
SNPdbe	rs753159426
MSV3d	rs753159426
GWAS Ctlg	rs753159426

Max Magnitude

0

ClinVar
Risk	rs753159426(-;-)
Alt	rs753159426(-;-)
Reference	Rs753159426(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000022.10:g.29091769delA
CLNSRC
CLNACC	RCV000234460.2, RCV000492286.1,