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rs63751081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751081(G;T)
Make rs63751081(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042272
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751081
ebirs63751081
HLIrs63751081
Exacrs63751081
Varsomers63751081
Maprs63751081
PheGenIrs63751081
hapmaprs63751081
1000 genomesrs63751081
hgdprs63751081
ensemblrs63751081
gopubmedrs63751081
geneviewrs63751081
scholarrs63751081
googlers63751081
pharmgkbrs63751081
gwascentralrs63751081
openSNPrs63751081
23andMers63751081
23andMe allrs63751081
SNP Nexus

SNPshotrs63751081
SNPdbers63751081
MSV3drs63751081
GWAS Ctlgrs63751081
Max Magnitude0
ClinVar
Risk rs63751081(T;T)
Alt rs63751081(T;T)
Reference rs63751081(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083763G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075309.2,