rs560596101

Orientation

plus

Stabilized

plus

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

Make rs560596101(A;C)

Make rs560596101(C;C)

Reference

GRCh38.p7 38.3/149

Chromosome

22

Position

28725241

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs560596101
dbSNP (classic)	rs560596101
ClinGen	rs560596101
ebi	rs560596101
HLI	rs560596101
Exac	rs560596101
Gnomad	rs560596101
Varsome	rs560596101
LitVar	rs560596101
Map	rs560596101
PheGenI	rs560596101
Biobank	rs560596101
1000 genomes	rs560596101
hgdp	rs560596101
ensembl	rs560596101
geneview	rs560596101
scholar	rs560596101
google	rs560596101
pharmgkb	rs560596101
gwascentral	rs560596101
openSNP	rs560596101
23andMe	rs560596101
SNPshot	rs560596101
SNPdbe	rs560596101
MSV3d	rs560596101
GWAS Ctlg	rs560596101

Max Magnitude

0

ClinVar
Risk	rs560596101(C;C) rs560596101(G;G) rs560596101(T;T)
Alt	rs560596101(C;C) rs560596101(G;G) rs560596101(T;T)
Reference	Rs560596101(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHEK2
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.29121229A>G
CLNSRC
CLNACC	RCV000483398.1,