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rs63751659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751659(-;-)
Make rs63751659(-;T)
Make rs63751659(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014437
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751659
ebirs63751659
HLIrs63751659
Exacrs63751659
Varsomers63751659
Maprs63751659
PheGenIrs63751659
hapmaprs63751659
1000 genomesrs63751659
hgdprs63751659
ensemblrs63751659
gopubmedrs63751659
geneviewrs63751659
scholarrs63751659
googlers63751659
pharmgkbrs63751659
gwascentralrs63751659
openSNPrs63751659
23andMers63751659
23andMe allrs63751659
SNP Nexus

SNPshotrs63751659
SNPdbers63751659
MSV3drs63751659
GWAS Ctlgrs63751659
Max Magnitude0
ClinVar
Risk rs63751659(T;T)
Alt rs63751659(T;T)
Reference rs63751659(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37055928dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075824.2,