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rs267607868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607868(-;-)
Make rs267607868(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047684
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607868
ebirs267607868
HLIrs267607868
Exacrs267607868
Varsomers267607868
Maprs267607868
PheGenIrs267607868
hapmaprs267607868
1000 genomesrs267607868
hgdprs267607868
ensemblrs267607868
gopubmedrs267607868
geneviewrs267607868
scholarrs267607868
googlers267607868
pharmgkbrs267607868
gwascentralrs267607868
openSNPrs267607868
23andMers267607868
23andMe allrs267607868
SNP Nexus

SNPshotrs267607868
SNPdbers267607868
MSV3drs267607868
GWAS Ctlgrs267607868
Max Magnitude0
ClinVar
Risk rs267607868(;)
Alt rs267607868(;)
Reference rs267607868(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089175delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075406.2,