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rs587778889

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778889(-;-)
Make rs587778889(-;A)
Make rs587778889(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025743
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778889
ebirs587778889
HLIrs587778889
Exacrs587778889
Varsomers587778889
Maprs587778889
PheGenIrs587778889
hapmaprs587778889
1000 genomesrs587778889
hgdprs587778889
ensemblrs587778889
gopubmedrs587778889
geneviewrs587778889
scholarrs587778889
googlers587778889
pharmgkbrs587778889
gwascentralrs587778889
openSNPrs587778889
23andMers587778889
23andMe allrs587778889
SNP Nexus

SNPshotrs587778889
SNPdbers587778889
MSV3drs587778889
GWAS Ctlgrs587778889
Max Magnitude0
ClinVar
Risk rs587778889(A;A)
Alt rs587778889(A;A)
Reference rs587778889(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067234dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075120.2,