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rs267607760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607760(A;G)
Make rs267607760(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37008908
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607760
ebirs267607760
HLIrs267607760
Exacrs267607760
Varsomers267607760
Maprs267607760
PheGenIrs267607760
hapmaprs267607760
1000 genomesrs267607760
hgdprs267607760
ensemblrs267607760
gopubmedrs267607760
geneviewrs267607760
scholarrs267607760
googlers267607760
pharmgkbrs267607760
gwascentralrs267607760
openSNPrs267607760
23andMers267607760
23andMe allrs267607760
SNP Nexus

SNPshotrs267607760
SNPdbers267607760
MSV3drs267607760
GWAS Ctlgrs267607760
Max Magnitude0
ClinVar
Risk rs267607760(G;G)
Alt rs267607760(G;G)
Reference rs267607760(A;A)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37050399A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075749.2, RCV000215515.1,