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rs267607873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGAGG;TGAGG) 0 common in clinvar
Make rs267607873(C;C)
Make rs267607873(C;TGAGG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048606
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607873
ebirs267607873
HLIrs267607873
Exacrs267607873
Varsomers267607873
Maprs267607873
PheGenIrs267607873
hapmaprs267607873
1000 genomesrs267607873
hgdprs267607873
ensemblrs267607873
gopubmedrs267607873
geneviewrs267607873
scholarrs267607873
googlers267607873
pharmgkbrs267607873
gwascentralrs267607873
openSNPrs267607873
23andMers267607873
23andMe allrs267607873
SNP Nexus

SNPshotrs267607873
SNPdbers267607873
MSV3drs267607873
GWAS Ctlgrs267607873
Max Magnitude0
ClinVar
Risk rs267607873(C;C)
Alt rs267607873(C;C)
Reference rs267607873(TGAGG;TGAGG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090097_37090101delTGAGGinsC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075451.2,