rs786201906

Orientation

minus

Stabilized

minus

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

Make rs786201906(A;A)

Make rs786201906(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

22

Position

28695243

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs786201906
dbSNP (classic)	rs786201906
ClinGen	rs786201906
ebi	rs786201906
HLI	rs786201906
Exac	rs786201906
Gnomad	rs786201906
Varsome	rs786201906
LitVar	rs786201906
Map	rs786201906
PheGenI	rs786201906
Biobank	rs786201906
1000 genomes	rs786201906
hgdp	rs786201906
ensembl	rs786201906
geneview	rs786201906
scholar	rs786201906
google	rs786201906
pharmgkb	rs786201906
gwascentral	rs786201906
openSNP	rs786201906
23andMe	rs786201906
SNPshot	rs786201906
SNPdbe	rs786201906
MSV3d	rs786201906
GWAS Ctlg	rs786201906

Max Magnitude

0

ClinVar
Risk	rs786201906(A;A)
Alt	rs786201906(A;A)
Reference	Rs786201906(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000022.10:g.29091231C>T
CLNSRC
CLNACC	RCV000164426.1,