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rs587778894

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778894(C;T)
Make rs587778894(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025769
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778894
ebirs587778894
HLIrs587778894
Exacrs587778894
Varsomers587778894
Maprs587778894
PheGenIrs587778894
hapmaprs587778894
1000 genomesrs587778894
hgdprs587778894
ensemblrs587778894
gopubmedrs587778894
geneviewrs587778894
scholarrs587778894
googlers587778894
pharmgkbrs587778894
gwascentralrs587778894
openSNPrs587778894
23andMers587778894
23andMe allrs587778894
SNP Nexus

SNPshotrs587778894
SNPdbers587778894
MSV3drs587778894
GWAS Ctlgrs587778894
Max Magnitude0
ClinVar
Risk rs587778894(T;T)
Alt rs587778894(T;T)
Reference rs587778894(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067260C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075144.3,