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rs587778939

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778939(-;-)
Make rs587778939(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37042268
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778939
ebirs587778939
HLIrs587778939
Exacrs587778939
Varsomers587778939
Maprs587778939
PheGenIrs587778939
hapmaprs587778939
1000 genomesrs587778939
hgdprs587778939
ensemblrs587778939
gopubmedrs587778939
geneviewrs587778939
scholarrs587778939
googlers587778939
pharmgkbrs587778939
gwascentralrs587778939
openSNPrs587778939
23andMers587778939
23andMe allrs587778939
SNP Nexus

SNPshotrs587778939
SNPdbers587778939
MSV3drs587778939
GWAS Ctlgrs587778939
Max Magnitude0
ClinVar
Risk rs587778939(;)
Alt rs587778939(;)
Reference rs587778939(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37083759delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075307.2,