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rs587779022

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779022(A;A)
Make rs587779022(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37011819
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779022
ebirs587779022
HLIrs587779022
Exacrs587779022
Varsomers587779022
Maprs587779022
PheGenIrs587779022
hapmaprs587779022
1000 genomesrs587779022
hgdprs587779022
ensemblrs587779022
gopubmedrs587779022
geneviewrs587779022
scholarrs587779022
googlers587779022
pharmgkbrs587779022
gwascentralrs587779022
openSNPrs587779022
23andMers587779022
23andMe allrs587779022
SNP Nexus

SNPshotrs587779022
SNPdbers587779022
MSV3drs587779022
GWAS Ctlgrs587779022
Max Magnitude0
ClinVar
Risk rs587779022(A;A)
Alt rs587779022(A;A)
Reference rs587779022(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053310G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075754.2,