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rs367543283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs367543283(-;-)
Make rs367543283(-;C)
Make rs367543283(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047545
GeneMLH1
is asnp
is mentioned by
dbSNPrs367543283
ebirs367543283
HLIrs367543283
Exacrs367543283
Varsomers367543283
Maprs367543283
PheGenIrs367543283
hapmaprs367543283
1000 genomesrs367543283
hgdprs367543283
ensemblrs367543283
gopubmedrs367543283
geneviewrs367543283
scholarrs367543283
googlers367543283
pharmgkbrs367543283
gwascentralrs367543283
openSNPrs367543283
23andMers367543283
23andMe allrs367543283
SNP Nexus

SNPshotrs367543283
SNPdbers367543283
MSV3drs367543283
GWAS Ctlgrs367543283
Max Magnitude0
ClinVar
Risk rs367543283(C;C)
Alt rs367543283(C;C)
Reference rs367543283(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089036dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075355.2,