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rs63751486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751486(-;-)
Make rs63751486(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047551
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751486
ebirs63751486
HLIrs63751486
Exacrs63751486
Varsomers63751486
Maprs63751486
PheGenIrs63751486
hapmaprs63751486
1000 genomesrs63751486
hgdprs63751486
ensemblrs63751486
gopubmedrs63751486
geneviewrs63751486
scholarrs63751486
googlers63751486
pharmgkbrs63751486
gwascentralrs63751486
openSNPrs63751486
23andMers63751486
23andMe allrs63751486
SNP Nexus

SNPshotrs63751486
SNPdbers63751486
MSV3drs63751486
GWAS Ctlgrs63751486
Max Magnitude0
ClinVar
Risk rs63751486(;)
Alt rs63751486(;)
Reference rs63751486(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089042delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075359.2,