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rs267607787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATG;AATG) 0 common in clinvar
Make rs267607787(-;-)
Make rs267607787(-;AATG)
ReferenceGRCh38 38.1/141
Chromosome3
Position37014481
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607787
ebirs267607787
HLIrs267607787
Exacrs267607787
Varsomers267607787
Maprs267607787
PheGenIrs267607787
hapmaprs267607787
1000 genomesrs267607787
hgdprs267607787
ensemblrs267607787
gopubmedrs267607787
geneviewrs267607787
scholarrs267607787
googlers267607787
pharmgkbrs267607787
gwascentralrs267607787
openSNPrs267607787
23andMers267607787
23andMe allrs267607787
SNP Nexus

SNPshotrs267607787
SNPdbers267607787
MSV3drs267607787
GWAS Ctlgrs267607787
Max Magnitude0
ClinVar
Risk rs267607787(;)
Alt rs267607787(;)
Reference rs267607787(AATG;AATG)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37055972_37055975delAATG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075829.2, RCV000220921.1,