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rs63749909

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63749909(C;C)
Make rs63749909(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37028891
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749909
ebirs63749909
HLIrs63749909
Exacrs63749909
Varsomers63749909
Maprs63749909
PheGenIrs63749909
hapmaprs63749909
1000 genomesrs63749909
hgdprs63749909
ensemblrs63749909
gopubmedrs63749909
geneviewrs63749909
scholarrs63749909
googlers63749909
pharmgkbrs63749909
gwascentralrs63749909
openSNPrs63749909
23andMers63749909
23andMe allrs63749909
SNP Nexus

SNPshotrs63749909
SNPdbers63749909
MSV3drs63749909
GWAS Ctlgrs63749909
Max Magnitude0
ClinVar
Risk rs63749909(C;C)
Alt rs63749909(C;C)
Reference rs63749909(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided not specified
Reversed 0
HGVS NC_000003.11:g.37070382T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075231.2, RCV000160534.4, RCV000174455.1, RCV000212539.1,