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rs267607877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607877(-;-)
Make rs267607877(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048608
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607877
ebirs267607877
HLIrs267607877
Exacrs267607877
Varsomers267607877
Maprs267607877
PheGenIrs267607877
hapmaprs267607877
1000 genomesrs267607877
hgdprs267607877
ensemblrs267607877
gopubmedrs267607877
geneviewrs267607877
scholarrs267607877
googlers267607877
pharmgkbrs267607877
gwascentralrs267607877
openSNPrs267607877
23andMers267607877
23andMe allrs267607877
SNP Nexus

SNPshotrs267607877
SNPdbers267607877
MSV3drs267607877
GWAS Ctlgrs267607877
Max Magnitude0
ClinVar
Risk rs267607877(;)
Alt rs267607877(;)
Reference rs267607877(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090099delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075454.2,