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rs267607897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCAGCTTGCTA;GCAGCTTGCTA) 0 common in clinvar
Make rs267607897(-;-)
Make rs267607897(-;GCAGCTTGCTA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050605
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607897
ebirs267607897
HLIrs267607897
Exacrs267607897
Varsomers267607897
Maprs267607897
PheGenIrs267607897
hapmaprs267607897
1000 genomesrs267607897
hgdprs267607897
ensemblrs267607897
gopubmedrs267607897
geneviewrs267607897
scholarrs267607897
googlers267607897
pharmgkbrs267607897
gwascentralrs267607897
openSNPrs267607897
23andMers267607897
23andMe allrs267607897
SNP Nexus

SNPshotrs267607897
SNPdbers267607897
MSV3drs267607897
GWAS Ctlgrs267607897
Max Magnitude0
ClinVar
Risk rs267607897(;)
Alt rs267607897(;)
Reference rs267607897(GCAGCTTGCTA;GCAGCTTGCTA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092096_37092106delGCAGCTTGCTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075579.2,