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rs748005072

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs748005072(-;-)
Make rs748005072(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position28703511
GeneCHEK2
is asnp
is mentioned by
dbSNPrs748005072
ebirs748005072
HLIrs748005072
Exacrs748005072
Varsomers748005072
Maprs748005072
PheGenIrs748005072
hapmaprs748005072
1000 genomesrs748005072
hgdprs748005072
ensemblrs748005072
gopubmedrs748005072
geneviewrs748005072
scholarrs748005072
googlers748005072
pharmgkbrs748005072
gwascentralrs748005072
openSNPrs748005072
23andMers748005072
23andMe allrs748005072
SNP Nexus

SNPshotrs748005072
SNPdbers748005072
MSV3drs748005072
GWAS Ctlgrs748005072
Max Magnitude0
ClinVar
Risk rs748005072(;)
Alt rs748005072(;)
Reference rs748005072(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CHEK2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000022.10:g.29099499delA
CLNSRC
CLNACC RCV000164458.1,