rs768384031

Orientation

plus

Stabilized

plus

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

Make rs768384031(A;A)

Make rs768384031(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

28734517

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs768384031
dbSNP (classic)	rs768384031
ClinGen	rs768384031
ebi	rs768384031
HLI	rs768384031
Exac	rs768384031
Gnomad	rs768384031
Varsome	rs768384031
LitVar	rs768384031
Map	rs768384031
PheGenI	rs768384031
Biobank	rs768384031
1000 genomes	rs768384031
hgdp	rs768384031
ensembl	rs768384031
geneview	rs768384031
scholar	rs768384031
google	rs768384031
pharmgkb	rs768384031
gwascentral	rs768384031
openSNP	rs768384031
23andMe	rs768384031
SNPshot	rs768384031
SNPdbe	rs768384031
MSV3d	rs768384031
GWAS Ctlg	rs768384031

Max Magnitude

0

ClinVar
Risk	rs768384031(A;A) rs768384031(T;T)
Alt	rs768384031(A;A) rs768384031(T;T)
Reference	Rs768384031(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	CHEK2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000022.10:g.29130505G>A
CLNSRC
CLNACC	RCV000218911.1, RCV000222824.1,