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rs1060502886

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs1060502886(-;-)
Make rs1060502886(-;TA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47799798
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502886
dbSNP (old)rs1060502886
ClinGenrs1060502886
ebirs1060502886
HLIrs1060502886
Exacrs1060502886
Gnomadrs1060502886
Varsomers1060502886
Maprs1060502886
PheGenIrs1060502886
Biobankrs1060502886
1000 genomesrs1060502886
hgdprs1060502886
ensemblrs1060502886
gopubmedrs1060502886
geneviewrs1060502886
scholarrs1060502886
googlers1060502886
pharmgkbrs1060502886
gwascentralrs1060502886
openSNPrs1060502886
23andMers1060502886
23andMe allrs1060502886
SNPshotrs1060502886
SNPdbers1060502886
MSV3drs1060502886
GWAS Ctlgrs1060502886
Max Magnitude0
ClinVar
Risk rs1060502886(-;-)
Alt rs1060502886(-;-)
Reference Rs1060502886(TA;TA)
Significance Pathogenic
Disease Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026937_48026938delTA
CLNSRC
CLNACC RCV000470844.1, RCV000486089.1, RCV000491721.1,