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rs63750386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750386(A;T)
Make rs63750386(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047597
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750386
ebirs63750386
HLIrs63750386
Exacrs63750386
Varsomers63750386
Maprs63750386
PheGenIrs63750386
hapmaprs63750386
1000 genomesrs63750386
hgdprs63750386
ensemblrs63750386
gopubmedrs63750386
geneviewrs63750386
scholarrs63750386
googlers63750386
pharmgkbrs63750386
gwascentralrs63750386
openSNPrs63750386
23andMers63750386
23andMe allrs63750386
SNP Nexus

SNPshotrs63750386
SNPdbers63750386
MSV3drs63750386
GWAS Ctlgrs63750386
Max Magnitude0
ClinVar
Risk rs63750386(T;T)
Alt rs63750386(T;T)
Reference rs63750386(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089088A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075370.2,