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rs587778947

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778947(-;-)
Make rs587778947(-;T)
Make rs587778947(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047608
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778947
ebirs587778947
HLIrs587778947
Exacrs587778947
Varsomers587778947
Maprs587778947
PheGenIrs587778947
hapmaprs587778947
1000 genomesrs587778947
hgdprs587778947
ensemblrs587778947
gopubmedrs587778947
geneviewrs587778947
scholarrs587778947
googlers587778947
pharmgkbrs587778947
gwascentralrs587778947
openSNPrs587778947
23andMers587778947
23andMe allrs587778947
SNP Nexus

SNPshotrs587778947
SNPdbers587778947
MSV3drs587778947
GWAS Ctlgrs587778947
Max Magnitude0
ClinVar
Risk rs587778947(T;T)
Alt rs587778947(T;T)
Reference rs587778947(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089099dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075373.2,