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rs63751247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
(GAA;GAA) 0 common in clinvar
Make rs63751247(-;-)
Make rs63751247(-;AAG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047639
GeneMLH1
is asnp
is mentioned by
dbSNPrs63751247
ebirs63751247
HLIrs63751247
Exacrs63751247
Varsomers63751247
Maprs63751247
PheGenIrs63751247
hapmaprs63751247
1000 genomesrs63751247
hgdprs63751247
ensemblrs63751247
gopubmedrs63751247
geneviewrs63751247
scholarrs63751247
googlers63751247
pharmgkbrs63751247
gwascentralrs63751247
openSNPrs63751247
23andMers63751247
23andMe allrs63751247
SNP Nexus

SNPshotrs63751247
SNPdbers63751247
MSV3drs63751247
GWAS Ctlgrs63751247
Max Magnitude0
ClinVar
Risk rs63751247(;)
Alt rs63751247(;)
Reference rs63751247(GAA;GAA)
Significance Pathogenic
Disease Turcot syndrome Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome II not provided
Variation info
Gene MLH1
CLNDBN Turcot syndrome Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome II not provided
Reversed 0
HGVS NC_000003.11:g.37089130_37089132delAAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000018609.27, RCV000075383.4, RCV000129328.4, RCV000192399.2, RCV000202279.2,