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rs587778898

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778898(-;-)
Make rs587778898(-;C)
Make rs587778898(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025808
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778898
ebirs587778898
HLIrs587778898
Exacrs587778898
Varsomers587778898
Maprs587778898
PheGenIrs587778898
hapmaprs587778898
1000 genomesrs587778898
hgdprs587778898
ensemblrs587778898
gopubmedrs587778898
geneviewrs587778898
scholarrs587778898
googlers587778898
pharmgkbrs587778898
gwascentralrs587778898
openSNPrs587778898
23andMers587778898
23andMe allrs587778898
SNP Nexus

SNPshotrs587778898
SNPdbers587778898
MSV3drs587778898
GWAS Ctlgrs587778898
Max Magnitude0
ClinVar
Risk rs587778898(C;C)
Alt rs587778898(C;C)
Reference rs587778898(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067299dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075151.2,