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rs267607823

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607823(A;G)
Make rs267607823(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position37025844
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607823
ebirs267607823
HLIrs267607823
Exacrs267607823
Varsomers267607823
Maprs267607823
PheGenIrs267607823
hapmaprs267607823
1000 genomesrs267607823
hgdprs267607823
ensemblrs267607823
gopubmedrs267607823
geneviewrs267607823
scholarrs267607823
googlers267607823
pharmgkbrs267607823
gwascentralrs267607823
openSNPrs267607823
23andMers267607823
23andMe allrs267607823
SNP Nexus

SNPshotrs267607823
SNPdbers267607823
MSV3drs267607823
GWAS Ctlgrs267607823
Max Magnitude0
ClinVar
Risk rs267607823(G;G)
Alt rs267607823(G;G)
Reference rs267607823(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067335A>G; NC_000003.11:g.37067335A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075158.2, RCV000205488.2,