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rs267607816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607816(C;C)
Make rs267607816(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020464
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607816
ebirs267607816
HLIrs267607816
Exacrs267607816
Varsomers267607816
Maprs267607816
PheGenIrs267607816
hapmaprs267607816
1000 genomesrs267607816
hgdprs267607816
ensemblrs267607816
gopubmedrs267607816
geneviewrs267607816
scholarrs267607816
googlers267607816
pharmgkbrs267607816
gwascentralrs267607816
openSNPrs267607816
23andMers267607816
23andMe allrs267607816
SNP Nexus

SNPshotrs267607816
SNPdbers267607816
MSV3drs267607816
GWAS Ctlgrs267607816
Max Magnitude0
ClinVar
Risk rs267607816(C;C)
Alt rs267607816(C;C)
Reference rs267607816(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061955G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075082.2,