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rs63749829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749829(G;T)
Make rs63749829(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000958
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749829
ebirs63749829
HLIrs63749829
Exacrs63749829
Varsomers63749829
Maprs63749829
PheGenIrs63749829
hapmaprs63749829
1000 genomesrs63749829
hgdprs63749829
ensemblrs63749829
gopubmedrs63749829
geneviewrs63749829
scholarrs63749829
googlers63749829
pharmgkbrs63749829
gwascentralrs63749829
openSNPrs63749829
23andMers63749829
23andMe allrs63749829
SNP Nexus

SNPshotrs63749829
SNPdbers63749829
MSV3drs63749829
GWAS Ctlgrs63749829
Max Magnitude0
ClinVar
Risk rs63749829(C,T;C,T)
Alt rs63749829(C,T;C,T)
Reference rs63749829(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042449G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075548.2,