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rs1060502937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502937(A;T)
Make rs1060502937(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47806623
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs1060502937
dbSNP (old)rs1060502937
ClinGenrs1060502937
ebirs1060502937
HLIrs1060502937
Exacrs1060502937
Gnomadrs1060502937
Varsomers1060502937
LitVarrs1060502937
Maprs1060502937
PheGenIrs1060502937
Biobankrs1060502937
1000 genomesrs1060502937
hgdprs1060502937
ensemblrs1060502937
gopubmedrs1060502937
geneviewrs1060502937
scholarrs1060502937
googlers1060502937
pharmgkbrs1060502937
gwascentralrs1060502937
openSNPrs1060502937
23andMers1060502937
23andMe allrs1060502937
SNPshotrs1060502937
SNPdbers1060502937
MSV3drs1060502937
GWAS Ctlgrs1060502937
Max Magnitude0
ClinVar
Risk rs1060502937(T;T)
Alt rs1060502937(T;T)
Reference Rs1060502937(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033762A>T
CLNSRC
CLNACC RCV000467214.1,