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rs1060502687

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1060502687(-;-)
Make rs1060502687(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28711917
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502687
dbSNP (old)rs1060502687
ClinGenrs1060502687
ebirs1060502687
HLIrs1060502687
Exacrs1060502687
Gnomadrs1060502687
Varsomers1060502687
Maprs1060502687
PheGenIrs1060502687
Biobankrs1060502687
1000 genomesrs1060502687
hgdprs1060502687
ensemblrs1060502687
gopubmedrs1060502687
geneviewrs1060502687
scholarrs1060502687
googlers1060502687
pharmgkbrs1060502687
gwascentralrs1060502687
openSNPrs1060502687
23andMers1060502687
23andMe allrs1060502687
SNPshotrs1060502687
SNPdbers1060502687
MSV3drs1060502687
GWAS Ctlgrs1060502687
Max Magnitude0
ClinVar
Risk rs1060502687(-;-)
Alt rs1060502687(-;-)
Reference Rs1060502687(AA;AA)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29107905_29107906delTT
CLNSRC
CLNACC RCV000457707.1,