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rs77120160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77120160(A;A)
Make rs77120160(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047500
GeneMLH1
is asnp
is mentioned by
dbSNPrs77120160
ebirs77120160
HLIrs77120160
Exacrs77120160
Varsomers77120160
Maprs77120160
PheGenIrs77120160
hapmaprs77120160
1000 genomesrs77120160
hgdprs77120160
ensemblrs77120160
gopubmedrs77120160
geneviewrs77120160
scholarrs77120160
googlers77120160
pharmgkbrs77120160
gwascentralrs77120160
openSNPrs77120160
23andMers77120160
23andMe allrs77120160
SNP Nexus

SNPshotrs77120160
SNPdbers77120160
MSV3drs77120160
GWAS Ctlgrs77120160
GMAF0.00551
Max Magnitude0
ClinVar
Risk rs77120160(A;A)
Alt rs77120160(A;A)
Reference rs77120160(T;T)
Significance Other
Disease Lynch syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37088991T>A
CLNSRC HGMD
CLNACC RCV000030216.3, RCV000078418.5,


[PMID 21056691OA-icon.png] Prevalence of alterations in DNA mismatch repair genes in patients with young-onset colorectal cancer.