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rs63751613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs63751613(-;-)
Make rs63751613(-;TT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040200
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751613
ebirs63751613
HLIrs63751613
Exacrs63751613
Varsomers63751613
Maprs63751613
PheGenIrs63751613
hapmaprs63751613
1000 genomesrs63751613
hgdprs63751613
ensemblrs63751613
gopubmedrs63751613
geneviewrs63751613
scholarrs63751613
googlers63751613
pharmgkbrs63751613
gwascentralrs63751613
openSNPrs63751613
23andMers63751613
23andMe allrs63751613
SNP Nexus

SNPshotrs63751613
SNPdbers63751613
MSV3drs63751613
GWAS Ctlgrs63751613
Max Magnitude0
ClinVar
Risk rs63751613(;)
Alt rs63751613(;)
Reference rs63751613(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081691_37081692delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075270.2,