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rs63750114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750114(A;A)
Make rs63750114(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37049015
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750114
ebirs63750114
HLIrs63750114
Exacrs63750114
Varsomers63750114
Maprs63750114
PheGenIrs63750114
hapmaprs63750114
1000 genomesrs63750114
hgdprs63750114
ensemblrs63750114
gopubmedrs63750114
geneviewrs63750114
scholarrs63750114
googlers63750114
pharmgkbrs63750114
gwascentralrs63750114
openSNPrs63750114
23andMers63750114
23andMe allrs63750114
SNP Nexus

SNPshotrs63750114
SNPdbers63750114
MSV3drs63750114
GWAS Ctlgrs63750114
GMAF0.002296
Max Magnitude0
ClinVar
Risk rs63750114(A,T;A,T)
Alt rs63750114(A,T;A,T)
Reference rs63750114(C;C)
Significance Other
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37090506C>A; NC_000003.11:g.37090506C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075527.2, RCV000130401.4, RCV000075528.2,