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rs1060502875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1060502875(-;-)
Make rs1060502875(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47791108
GeneMSH6
is asnp
is mentioned by
dbSNPrs1060502875
dbSNP (old)rs1060502875
ClinGenrs1060502875
ebirs1060502875
HLIrs1060502875
Exacrs1060502875
Gnomadrs1060502875
Varsomers1060502875
Maprs1060502875
PheGenIrs1060502875
Biobankrs1060502875
1000 genomesrs1060502875
hgdprs1060502875
ensemblrs1060502875
gopubmedrs1060502875
geneviewrs1060502875
scholarrs1060502875
googlers1060502875
pharmgkbrs1060502875
gwascentralrs1060502875
openSNPrs1060502875
23andMers1060502875
23andMe allrs1060502875
SNPshotrs1060502875
SNPdbers1060502875
MSV3drs1060502875
GWAS Ctlgrs1060502875
Max Magnitude0
ClinVar
Risk rs1060502875(-;-)
Alt rs1060502875(-;-)
Reference Rs1060502875(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48018247_48018248delTT
CLNSRC
CLNACC RCV000463357.1,