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rs63750486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTG;TTG) 0 common in clinvar
Make rs63750486(-;-)
Make rs63750486(-;TTG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047622
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750486
ebirs63750486
HLIrs63750486
Exacrs63750486
Varsomers63750486
Maprs63750486
PheGenIrs63750486
hapmaprs63750486
1000 genomesrs63750486
hgdprs63750486
ensemblrs63750486
gopubmedrs63750486
geneviewrs63750486
scholarrs63750486
googlers63750486
pharmgkbrs63750486
gwascentralrs63750486
openSNPrs63750486
23andMers63750486
23andMe allrs63750486
SNP Nexus

SNPshotrs63750486
SNPdbers63750486
MSV3drs63750486
GWAS Ctlgrs63750486
Max Magnitude0
ClinVar
Risk rs63750486(;)
Alt rs63750486(;)
Reference rs63750486(TTG;TTG)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089113_37089115delTTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075377.2,