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rs1060500706

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500706(-;-)
Make rs1060500706(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37050518
GeneMLH1
is asnp
is mentioned by
dbSNPrs1060500706
dbSNP (old)rs1060500706
ClinGenrs1060500706
ebirs1060500706
HLIrs1060500706
Exacrs1060500706
Gnomadrs1060500706
Varsomers1060500706
Maprs1060500706
PheGenIrs1060500706
Biobankrs1060500706
1000 genomesrs1060500706
hgdprs1060500706
ensemblrs1060500706
gopubmedrs1060500706
geneviewrs1060500706
scholarrs1060500706
googlers1060500706
pharmgkbrs1060500706
gwascentralrs1060500706
openSNPrs1060500706
23andMers1060500706
23andMe allrs1060500706
SNPshotrs1060500706
SNPdbers1060500706
MSV3drs1060500706
GWAS Ctlgrs1060500706
Max Magnitude0
ClinVar
Risk rs1060500706(-;-)
Alt rs1060500706(-;-)
Reference Rs1060500706(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092009delG
CLNSRC
CLNACC RCV000458600.1,