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rs63750859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs63750859(-;-)
Make rs63750859(-;TC)
ReferenceGRCh38 38.1/141
Chromosome3
Position37049006
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750859
ebirs63750859
HLIrs63750859
Exacrs63750859
Varsomers63750859
Maprs63750859
PheGenIrs63750859
hapmaprs63750859
1000 genomesrs63750859
hgdprs63750859
ensemblrs63750859
gopubmedrs63750859
geneviewrs63750859
scholarrs63750859
googlers63750859
pharmgkbrs63750859
gwascentralrs63750859
openSNPrs63750859
23andMers63750859
23andMe allrs63750859
SNP Nexus

SNPshotrs63750859
SNPdbers63750859
MSV3drs63750859
GWAS Ctlgrs63750859
Max Magnitude0
ClinVar
Risk rs63750859(;)
Alt rs63750859(;)
Reference rs63750859(CT;CT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090497_37090498delTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075524.2,