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rs63751689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751689(-;-)
Make rs63751689(-;T)
Make rs63751689(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028928
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751689
ebirs63751689
HLIrs63751689
Exacrs63751689
Varsomers63751689
Maprs63751689
PheGenIrs63751689
hapmaprs63751689
1000 genomesrs63751689
hgdprs63751689
ensemblrs63751689
gopubmedrs63751689
geneviewrs63751689
scholarrs63751689
googlers63751689
pharmgkbrs63751689
gwascentralrs63751689
openSNPrs63751689
23andMers63751689
23andMe allrs63751689
SNP Nexus

SNPshotrs63751689
SNPdbers63751689
MSV3drs63751689
GWAS Ctlgrs63751689
Max Magnitude0
ClinVar
Risk rs63751689(T;T)
Alt rs63751689(T;T)
Reference rs63751689(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070419dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075242.2,