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rs63749795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749795(C;T)
Make rs63749795(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028833
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749795
ebirs63749795
HLIrs63749795
Exacrs63749795
Varsomers63749795
Maprs63749795
PheGenIrs63749795
hapmaprs63749795
1000 genomesrs63749795
hgdprs63749795
ensemblrs63749795
gopubmedrs63749795
geneviewrs63749795
scholarrs63749795
googlers63749795
pharmgkbrs63749795
gwascentralrs63749795
openSNPrs63749795
23andMers63749795
23andMe allrs63749795
SNP Nexus

SNPshotrs63749795
SNPdbers63749795
MSV3drs63749795
GWAS Ctlgrs63749795
Max Magnitude0
ClinVar
Risk rs63749795(T;T)
Alt rs63749795(T;T)
Reference rs63749795(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37070324C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075218.3, RCV000128870.2,