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rs63750020

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750020(-;-)
Make rs63750020(-;A)
Make rs63750020(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025975
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750020
ebirs63750020
HLIrs63750020
Exacrs63750020
Varsomers63750020
Maprs63750020
PheGenIrs63750020
hapmaprs63750020
1000 genomesrs63750020
hgdprs63750020
ensemblrs63750020
gopubmedrs63750020
geneviewrs63750020
scholarrs63750020
googlers63750020
pharmgkbrs63750020
gwascentralrs63750020
openSNPrs63750020
23andMers63750020
23andMe allrs63750020
SNP Nexus

SNPshotrs63750020
SNPdbers63750020
MSV3drs63750020
GWAS Ctlgrs63750020
Max Magnitude0
ClinVar
Risk rs63750020(A;A)
Alt rs63750020(A;A)
Reference rs63750020(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067466dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075183.2,