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rs1060500689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500689(C;G)
Make rs1060500689(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37007000
GeneMLH1
is asnp
is mentioned by
dbSNPrs1060500689
dbSNP (old)rs1060500689
ClinGenrs1060500689
ebirs1060500689
HLIrs1060500689
Exacrs1060500689
Gnomadrs1060500689
Varsomers1060500689
LitVarrs1060500689
Maprs1060500689
PheGenIrs1060500689
Biobankrs1060500689
1000 genomesrs1060500689
hgdprs1060500689
ensemblrs1060500689
gopubmedrs1060500689
geneviewrs1060500689
scholarrs1060500689
googlers1060500689
pharmgkbrs1060500689
gwascentralrs1060500689
openSNPrs1060500689
23andMers1060500689
23andMe allrs1060500689
SNPshotrs1060500689
SNPdbers1060500689
MSV3drs1060500689
GWAS Ctlgrs1060500689
Max Magnitude0
ClinVar
Risk rs1060500689(G;G)
Alt rs1060500689(G;G)
Reference Rs1060500689(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048491C>G
CLNSRC
CLNACC RCV000470067.1,