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rs63750034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs63750034(-;-)
Make rs63750034(-;AA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017574
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750034
ebirs63750034
HLIrs63750034
Exacrs63750034
Varsomers63750034
Maprs63750034
PheGenIrs63750034
hapmaprs63750034
1000 genomesrs63750034
hgdprs63750034
ensemblrs63750034
gopubmedrs63750034
geneviewrs63750034
scholarrs63750034
googlers63750034
pharmgkbrs63750034
gwascentralrs63750034
openSNPrs63750034
23andMers63750034
23andMe allrs63750034
SNP Nexus

SNPshotrs63750034
SNPdbers63750034
MSV3drs63750034
GWAS Ctlgrs63750034
Max Magnitude0
ClinVar
Risk rs63750034(;)
Alt rs63750034(;)
Reference rs63750034(AA;AA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059065_37059066delAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075889.2,