rs137853008

Orientation

minus

Stabilized

minus

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

Make rs137853008(G;T)

Make rs137853008(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

28734673

Gene

CHEK2

is a	snp
is	mentioned by
dbSNP	rs137853008
dbSNP (classic)	rs137853008
ClinGen	rs137853008
ebi	rs137853008
HLI	rs137853008
Exac	rs137853008
Gnomad	rs137853008
Varsome	rs137853008
LitVar	rs137853008
Map	rs137853008
PheGenI	rs137853008
Biobank	rs137853008
1000 genomes	rs137853008
hgdp	rs137853008
ensembl	rs137853008
geneview	rs137853008
scholar	rs137853008
google	rs137853008
pharmgkb	rs137853008
gwascentral	rs137853008
openSNP	rs137853008
23andMe	rs137853008
SNPshot	rs137853008
SNPdbe	rs137853008
MSV3d	rs137853008
GWAS Ctlg	rs137853008

Max Magnitude

0

OMIM	604373
Desc
Variant	0006
Related	also

ClinVar
Risk	rs137853008(T;T)
Alt	rs137853008(T;T)
Reference	Rs137853008(G;G)
Significance	Pathogenic
Disease	Osteosarcoma
Variation	info
Gene	CHEK2
CLNDBN	Osteosarcoma
Reversed	1
HGVS	NC_000022.10:g.29130661C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005943.5,