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rs587779042

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779042(A;A)
Make rs587779042(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017499
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779042
ebirs587779042
HLIrs587779042
Exacrs587779042
Varsomers587779042
Maprs587779042
PheGenIrs587779042
hapmaprs587779042
1000 genomesrs587779042
hgdprs587779042
ensemblrs587779042
gopubmedrs587779042
geneviewrs587779042
scholarrs587779042
googlers587779042
pharmgkbrs587779042
gwascentralrs587779042
openSNPrs587779042
23andMers587779042
23andMe allrs587779042
SNP Nexus

SNPshotrs587779042
SNPdbers587779042
MSV3drs587779042
GWAS Ctlgrs587779042
Max Magnitude0
ClinVar
Risk rs587779042(A;A)
Alt rs587779042(A;A)
Reference rs587779042(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37058990T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075866.2,