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rs267607821

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607821(-;-)
Make rs267607821(-;G)
Make rs267607821(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025960
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607821
ebirs267607821
HLIrs267607821
Exacrs267607821
Varsomers267607821
Maprs267607821
PheGenIrs267607821
hapmaprs267607821
1000 genomesrs267607821
hgdprs267607821
ensemblrs267607821
gopubmedrs267607821
geneviewrs267607821
scholarrs267607821
googlers267607821
pharmgkbrs267607821
gwascentralrs267607821
openSNPrs267607821
23andMers267607821
23andMe allrs267607821
SNP Nexus

SNPshotrs267607821
SNPdbers267607821
MSV3drs267607821
GWAS Ctlgrs267607821
Max Magnitude0
ClinVar
Risk rs267607821(G;G)
Alt rs267607821(G;G)
Reference rs267607821(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067451dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075181.2,