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rs587779052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779052(-;-)
Make rs587779052(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37020326
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779052
dbSNP (old)rs587779052
ClinGenrs587779052
ebirs587779052
HLIrs587779052
Exacrs587779052
Gnomadrs587779052
Varsomers587779052
Maprs587779052
PheGenIrs587779052
Biobankrs587779052
1000 genomesrs587779052
hgdprs587779052
ensemblrs587779052
gopubmedrs587779052
geneviewrs587779052
scholarrs587779052
googlers587779052
pharmgkbrs587779052
gwascentralrs587779052
openSNPrs587779052
23andMers587779052
23andMe allrs587779052
SNP Nexus

SNPshotrs587779052
SNPdbers587779052
MSV3drs587779052
GWAS Ctlgrs587779052
Max Magnitude0
ClinVar
Risk rs587779052(-;-)
Alt rs587779052(-;-)
Reference Rs587779052(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061817delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075929.2,