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

rs587779009

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779009(-;-)
Make rs587779009(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37006998
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779009
ebirs587779009
HLIrs587779009
Exacrs587779009
Varsomers587779009
Maprs587779009
PheGenIrs587779009
hapmaprs587779009
1000 genomesrs587779009
hgdprs587779009
ensemblrs587779009
gopubmedrs587779009
geneviewrs587779009
scholarrs587779009
googlers587779009
pharmgkbrs587779009
gwascentralrs587779009
openSNPrs587779009
23andMers587779009
23andMe allrs587779009
SNP Nexus

SNPshotrs587779009
SNPdbers587779009
MSV3drs587779009
GWAS Ctlgrs587779009
Max Magnitude0
ClinVar
Risk rs587779009(;)
Alt rs587779009(;)
Reference rs587779009(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048489delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075692.2,