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rs587779033

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779033(-;-)
Make rs587779033(-;T)
Make rs587779033(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37012099
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779033
ebirs587779033
HLIrs587779033
Exacrs587779033
Varsomers587779033
Maprs587779033
PheGenIrs587779033
hapmaprs587779033
1000 genomesrs587779033
hgdprs587779033
ensemblrs587779033
gopubmedrs587779033
geneviewrs587779033
scholarrs587779033
googlers587779033
pharmgkbrs587779033
gwascentralrs587779033
openSNPrs587779033
23andMers587779033
23andMe allrs587779033
SNP Nexus

SNPshotrs587779033
SNPdbers587779033
MSV3drs587779033
GWAS Ctlgrs587779033
Max Magnitude0
ClinVar
Risk rs587779033(T;T)
Alt rs587779033(T;T)
Reference rs587779033(;)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053590_37053591insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075812.2,