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rs1060502888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1060502888(-;-)
Make rs1060502888(-;CA)
Make rs1060502888(CA;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47798856
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502888
dbSNP (old)rs1060502888
ClinGenrs1060502888
ebirs1060502888
HLIrs1060502888
Exacrs1060502888
Gnomadrs1060502888
Varsomers1060502888
Maprs1060502888
PheGenIrs1060502888
Biobankrs1060502888
1000 genomesrs1060502888
hgdprs1060502888
ensemblrs1060502888
gopubmedrs1060502888
geneviewrs1060502888
scholarrs1060502888
googlers1060502888
pharmgkbrs1060502888
gwascentralrs1060502888
openSNPrs1060502888
23andMers1060502888
23andMe allrs1060502888
SNPshotrs1060502888
SNPdbers1060502888
MSV3drs1060502888
GWAS Ctlgrs1060502888
Max Magnitude0
ClinVar
Risk rs1060502888(-;-)
Alt rs1060502888(-;-)
Reference Rs1060502888(AC;AC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025995_48025996delCA
CLNSRC
CLNACC RCV000473969.1,