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rs63749867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749867(C;T)
Make rs63749867(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048954
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749867
ebirs63749867
HLIrs63749867
Exacrs63749867
Varsomers63749867
Maprs63749867
PheGenIrs63749867
hapmaprs63749867
1000 genomesrs63749867
hgdprs63749867
ensemblrs63749867
gopubmedrs63749867
geneviewrs63749867
scholarrs63749867
googlers63749867
pharmgkbrs63749867
gwascentralrs63749867
openSNPrs63749867
23andMers63749867
23andMe allrs63749867
SNP Nexus

SNPshotrs63749867
SNPdbers63749867
MSV3drs63749867
GWAS Ctlgrs63749867
Max Magnitude0
ClinVar
Risk rs63749867(A,T;A,T)
Alt rs63749867(A,T;A,T)
Reference rs63749867(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090445C>A; NC_000003.11:g.37090445C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075493.2, RCV000075494.2,