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rs63750903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGG;TGG) 0 common in clinvar
Make rs63750903(CT;CT)
Make rs63750903(CT;GG)
Make rs63750903(GG;GG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008891
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750903
ebirs63750903
HLIrs63750903
Exacrs63750903
Varsomers63750903
Maprs63750903
PheGenIrs63750903
hapmaprs63750903
1000 genomesrs63750903
hgdprs63750903
ensemblrs63750903
gopubmedrs63750903
geneviewrs63750903
scholarrs63750903
googlers63750903
pharmgkbrs63750903
gwascentralrs63750903
openSNPrs63750903
23andMers63750903
23andMe allrs63750903
SNP Nexus

SNPshotrs63750903
SNPdbers63750903
MSV3drs63750903
GWAS Ctlgrs63750903
Max Magnitude0
ClinVar
Risk rs63750903(TAT,TCT;TAT,TCT)
Alt rs63750903(TAT,TCT;TAT,TCT)
Reference rs63750903(TGG;TGG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050382_37050383delGGinsAT; NC_000003.11:g.37050382_37050383delGGinsCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075744.2, RCV000075745.2,