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rs267607720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607720(C;G)
Make rs267607720(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000952
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607720
ebirs267607720
HLIrs267607720
Exacrs267607720
Varsomers267607720
Maprs267607720
PheGenIrs267607720
hapmaprs267607720
1000 genomesrs267607720
hgdprs267607720
ensemblrs267607720
gopubmedrs267607720
geneviewrs267607720
scholarrs267607720
googlers267607720
pharmgkbrs267607720
gwascentralrs267607720
openSNPrs267607720
23andMers267607720
23andMe allrs267607720
SNP Nexus

SNPshotrs267607720
SNPdbers267607720
MSV3drs267607720
GWAS Ctlgrs267607720
Max Magnitude0
ClinVar
Risk rs267607720(G;G)
Alt rs267607720(G;G)
Reference rs267607720(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37042443C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075517.2, RCV000160554.2,