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rs63750464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750464(-;-)
Make rs63750464(-;A)
Make rs63750464(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37042289
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750464
ebirs63750464
HLIrs63750464
Exacrs63750464
Varsomers63750464
Maprs63750464
PheGenIrs63750464
hapmaprs63750464
1000 genomesrs63750464
hgdprs63750464
ensemblrs63750464
gopubmedrs63750464
geneviewrs63750464
scholarrs63750464
googlers63750464
pharmgkbrs63750464
gwascentralrs63750464
openSNPrs63750464
23andMers63750464
23andMe allrs63750464
SNP Nexus

SNPshotrs63750464
SNPdbers63750464
MSV3drs63750464
GWAS Ctlgrs63750464
Max Magnitude0
ClinVar
Risk rs63750464(A;A)
Alt rs63750464(A;A)
Reference rs63750464(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083780dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075314.2,