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rs1060502684

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs1060502684(-;-)
Make rs1060502684(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position28695829
GeneCHEK2
is asnp
is mentioned by
dbSNPrs1060502684
dbSNP (old)rs1060502684
ClinGenrs1060502684
ebirs1060502684
HLIrs1060502684
Exacrs1060502684
Gnomadrs1060502684
Varsomers1060502684
Maprs1060502684
PheGenIrs1060502684
Biobankrs1060502684
1000 genomesrs1060502684
hgdprs1060502684
ensemblrs1060502684
gopubmedrs1060502684
geneviewrs1060502684
scholarrs1060502684
googlers1060502684
pharmgkbrs1060502684
gwascentralrs1060502684
openSNPrs1060502684
23andMers1060502684
23andMe allrs1060502684
SNPshotrs1060502684
SNPdbers1060502684
MSV3drs1060502684
GWAS Ctlgrs1060502684
Max Magnitude0
ClinVar
Risk rs1060502684(-;-)
Alt rs1060502684(-;-)
Reference Rs1060502684(TC;TC)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene CHEK2
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000022.10:g.29091817_29091818delGA
CLNSRC
CLNACC RCV000469025.1,