Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779031

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779031(-;-)
Make rs587779031(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37012094
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779031
ebirs587779031
HLIrs587779031
Exacrs587779031
Varsomers587779031
Maprs587779031
PheGenIrs587779031
hapmaprs587779031
1000 genomesrs587779031
hgdprs587779031
ensemblrs587779031
gopubmedrs587779031
geneviewrs587779031
scholarrs587779031
googlers587779031
pharmgkbrs587779031
gwascentralrs587779031
openSNPrs587779031
23andMers587779031
23andMe allrs587779031
SNP Nexus

SNPshotrs587779031
SNPdbers587779031
MSV3drs587779031
GWAS Ctlgrs587779031
Max Magnitude0
ClinVar
Risk rs587779031(;)
Alt rs587779031(;)
Reference rs587779031(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053585delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075799.2,