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rs587779024

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779024(A;A)
Make rs587779024(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37011864
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779024
ebirs587779024
HLIrs587779024
Exacrs587779024
Varsomers587779024
Maprs587779024
PheGenIrs587779024
hapmaprs587779024
1000 genomesrs587779024
hgdprs587779024
ensemblrs587779024
gopubmedrs587779024
geneviewrs587779024
scholarrs587779024
googlers587779024
pharmgkbrs587779024
gwascentralrs587779024
openSNPrs587779024
23andMers587779024
23andMe allrs587779024
SNP Nexus

SNPshotrs587779024
SNPdbers587779024
MSV3drs587779024
GWAS Ctlgrs587779024
Max Magnitude0
ClinVar
Risk rs587779024(A;A)
Alt rs587779024(A;A)
Reference rs587779024(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053355T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075771.2,