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rs63749990

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63749990(G;G)
Make rs63749990(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000985
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749990
ebirs63749990
HLIrs63749990
Exacrs63749990
Varsomers63749990
Maprs63749990
PheGenIrs63749990
hapmaprs63749990
1000 genomesrs63749990
hgdprs63749990
ensemblrs63749990
gopubmedrs63749990
geneviewrs63749990
scholarrs63749990
googlers63749990
pharmgkbrs63749990
gwascentralrs63749990
openSNPrs63749990
23andMers63749990
23andMe allrs63749990
SNP Nexus

SNPshotrs63749990
SNPdbers63749990
MSV3drs63749990
GWAS Ctlgrs63749990
Max Magnitude0
ClinVar
Risk rs63749990(G;G)
Alt rs63749990(G;G)
Reference rs63749990(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042476T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075601.2,