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rs63750309

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750309(-;-)
Make rs63750309(-;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047536
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750309
ebirs63750309
HLIrs63750309
Exacrs63750309
Varsomers63750309
Maprs63750309
PheGenIrs63750309
hapmaprs63750309
1000 genomesrs63750309
hgdprs63750309
ensemblrs63750309
gopubmedrs63750309
geneviewrs63750309
scholarrs63750309
googlers63750309
pharmgkbrs63750309
gwascentralrs63750309
openSNPrs63750309
23andMers63750309
23andMe allrs63750309
SNP Nexus

SNPshotrs63750309
SNPdbers63750309
MSV3drs63750309
GWAS Ctlgrs63750309
Max Magnitude0
ClinVar
Risk rs63750309(;)
Alt rs63750309(;)
Reference rs63750309(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089027delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075350.2,