rs536907995

Orientation

plus

Stabilized

plus

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

Make rs536907995(A;A)

Make rs536907995(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

22

Position

28734664

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs536907995
dbSNP (classic)	rs536907995
ClinGen	rs536907995
ebi	rs536907995
HLI	rs536907995
Exac	rs536907995
Gnomad	rs536907995
Varsome	rs536907995
LitVar	rs536907995
Map	rs536907995
PheGenI	rs536907995
Biobank	rs536907995
1000 genomes	rs536907995
hgdp	rs536907995
ensembl	rs536907995
geneview	rs536907995
scholar	rs536907995
google	rs536907995
pharmgkb	rs536907995
gwascentral	rs536907995
openSNP	rs536907995
23andMe	rs536907995
SNPshot	rs536907995
SNPdbe	rs536907995
MSV3d	rs536907995
GWAS Ctlg	rs536907995

Max Magnitude

0

ClinVar
Risk	rs536907995(A;A)
Alt	rs536907995(A;A)
Reference	Rs536907995(G;G)
Significance	Pathogenic
Disease	not specified not provided Familial cancer of breast
Variation	info
Gene	CHEK2
CLNDBN	not specified not provided Familial cancer of breast
Reversed	0
HGVS	NC_000022.10:g.29130652G>A
CLNSRC
CLNACC	RCV000120552.1, RCV000255024.1, RCV000458969.1,