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rs587778989

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778989(-;-)
Make rs587778989(-;A)
Make rs587778989(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050600
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778989
ebirs587778989
HLIrs587778989
Exacrs587778989
Varsomers587778989
Maprs587778989
PheGenIrs587778989
hapmaprs587778989
1000 genomesrs587778989
hgdprs587778989
ensemblrs587778989
gopubmedrs587778989
geneviewrs587778989
scholarrs587778989
googlers587778989
pharmgkbrs587778989
gwascentralrs587778989
openSNPrs587778989
23andMers587778989
23andMe allrs587778989
SNP Nexus

SNPshotrs587778989
SNPdbers587778989
MSV3drs587778989
GWAS Ctlgrs587778989
Max Magnitude0
ClinVar
Risk rs587778989(A;A)
Alt rs587778989(A;A)
Reference rs587778989(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092091dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075577.2,