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rs63750814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750814(-;-)
Make rs63750814(-;A)
Make rs63750814(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017575
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750814
ebirs63750814
HLIrs63750814
Exacrs63750814
Varsomers63750814
Maprs63750814
PheGenIrs63750814
hapmaprs63750814
1000 genomesrs63750814
hgdprs63750814
ensemblrs63750814
gopubmedrs63750814
geneviewrs63750814
scholarrs63750814
googlers63750814
pharmgkbrs63750814
gwascentralrs63750814
openSNPrs63750814
23andMers63750814
23andMe allrs63750814
SNP Nexus

SNPshotrs63750814
SNPdbers63750814
MSV3drs63750814
GWAS Ctlgrs63750814
Max Magnitude0
ClinVar
Risk rs63750814(A;A)
Alt rs63750814(A;A)
Reference rs63750814(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059066dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075892.2,