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rs267607809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607809(-;-)
Make rs267607809(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37020313
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607809
ebirs267607809
HLIrs267607809
Exacrs267607809
Varsomers267607809
Maprs267607809
PheGenIrs267607809
hapmaprs267607809
1000 genomesrs267607809
hgdprs267607809
ensemblrs267607809
gopubmedrs267607809
geneviewrs267607809
scholarrs267607809
googlers267607809
pharmgkbrs267607809
gwascentralrs267607809
openSNPrs267607809
23andMers267607809
23andMe allrs267607809
SNP Nexus

SNPshotrs267607809
SNPdbers267607809
MSV3drs267607809
GWAS Ctlgrs267607809
Max Magnitude0
ClinVar
Risk rs267607809(;)
Alt rs267607809(;)
Reference rs267607809(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061804delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075925.2,