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rs1060502898

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1060502898(-;T)
Make rs1060502898(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47806858
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs1060502898
dbSNP (old)rs1060502898
ClinGenrs1060502898
ebirs1060502898
HLIrs1060502898
Exacrs1060502898
Gnomadrs1060502898
Varsomers1060502898
Maprs1060502898
PheGenIrs1060502898
Biobankrs1060502898
1000 genomesrs1060502898
hgdprs1060502898
ensemblrs1060502898
gopubmedrs1060502898
geneviewrs1060502898
scholarrs1060502898
googlers1060502898
pharmgkbrs1060502898
gwascentralrs1060502898
openSNPrs1060502898
23andMers1060502898
23andMe allrs1060502898
SNPshotrs1060502898
SNPdbers1060502898
MSV3drs1060502898
GWAS Ctlgrs1060502898
Max Magnitude0
ClinVar
Risk rs1060502898(T;T) rs1060502898(TAT;TAT)
Alt rs1060502898(T;T) rs1060502898(TAT;TAT)
Reference Rs1060502898(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033969_48033997dup
CLNSRC
CLNACC RCV000491731.1,