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rs267607723

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAA;AGAA) 0 common in clinvar
Make rs267607723(-;-)
Make rs267607723(-;AGAA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000957
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607723
ebirs267607723
HLIrs267607723
Exacrs267607723
Varsomers267607723
Maprs267607723
PheGenIrs267607723
hapmaprs267607723
1000 genomesrs267607723
hgdprs267607723
ensemblrs267607723
gopubmedrs267607723
geneviewrs267607723
scholarrs267607723
googlers267607723
pharmgkbrs267607723
gwascentralrs267607723
openSNPrs267607723
23andMers267607723
23andMe allrs267607723
SNP Nexus

SNPshotrs267607723
SNPdbers267607723
MSV3drs267607723
GWAS Ctlgrs267607723
Max Magnitude0
ClinVar
Risk rs267607723(;)
Alt rs267607723(;)
Reference rs267607723(AGAA;AGAA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042448_37042451delAGAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075546.2,