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rs267607778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607778(G;T)
Make rs267607778(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37012100
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607778
ebirs267607778
HLIrs267607778
Exacrs267607778
Varsomers267607778
Maprs267607778
PheGenIrs267607778
hapmaprs267607778
1000 genomesrs267607778
hgdprs267607778
ensemblrs267607778
gopubmedrs267607778
geneviewrs267607778
scholarrs267607778
googlers267607778
pharmgkbrs267607778
gwascentralrs267607778
openSNPrs267607778
23andMers267607778
23andMe allrs267607778
SNP Nexus

SNPshotrs267607778
SNPdbers267607778
MSV3drs267607778
GWAS Ctlgrs267607778
Max Magnitude0
ClinVar
Risk rs267607778(A,T;A,T)
Alt rs267607778(A,T;A,T)
Reference rs267607778(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37053591G>A; NC_000003.11:g.37053591G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075802.2, RCV000075803.2,