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rs137853008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853008(G;T)
Make rs137853008(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position28734673
GeneCHEK2
is asnp
is mentioned by
dbSNPrs137853008
ebirs137853008
HLIrs137853008
Exacrs137853008
Varsomers137853008
Maprs137853008
PheGenIrs137853008
hapmaprs137853008
1000 genomesrs137853008
hgdprs137853008
ensemblrs137853008
gopubmedrs137853008
geneviewrs137853008
scholarrs137853008
googlers137853008
pharmgkbrs137853008
gwascentralrs137853008
openSNPrs137853008
23andMers137853008
23andMe allrs137853008
SNP Nexus

SNPshotrs137853008
SNPdbers137853008
MSV3drs137853008
GWAS Ctlgrs137853008
Max Magnitude0
OMIM604373
Desc
Variant0006
Relatedalso
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
CLNACC RCV000005943.5,