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rs63749923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749923(C;T)
Make rs63749923(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028902
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749923
ebirs63749923
HLIrs63749923
Exacrs63749923
Varsomers63749923
Maprs63749923
PheGenIrs63749923
hapmaprs63749923
1000 genomesrs63749923
hgdprs63749923
ensemblrs63749923
gopubmedrs63749923
geneviewrs63749923
scholarrs63749923
googlers63749923
pharmgkbrs63749923
gwascentralrs63749923
openSNPrs63749923
23andMers63749923
23andMe allrs63749923
SNP Nexus

SNPshotrs63749923
SNPdbers63749923
MSV3drs63749923
GWAS Ctlgrs63749923
Max Magnitude0
ClinVar
Risk rs63749923(T;T)
Alt rs63749923(T;T)
Reference rs63749923(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070393C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075235.2,