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rs267607801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACTT;ACTT) 0 common in clinvar
Make rs267607801(-;-)
Make rs267607801(-;ACTT)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017523
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607801
ebirs267607801
HLIrs267607801
Exacrs267607801
Varsomers267607801
Maprs267607801
PheGenIrs267607801
hapmaprs267607801
1000 genomesrs267607801
hgdprs267607801
ensemblrs267607801
gopubmedrs267607801
geneviewrs267607801
scholarrs267607801
googlers267607801
pharmgkbrs267607801
gwascentralrs267607801
openSNPrs267607801
23andMers267607801
23andMe allrs267607801
SNP Nexus

SNPshotrs267607801
SNPdbers267607801
MSV3drs267607801
GWAS Ctlgrs267607801
Max Magnitude0
ClinVar
Risk rs267607801(;)
Alt rs267607801(;)
Reference rs267607801(ACTT;ACTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059014_37059017delACTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075876.2,