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rs267607883

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607883(A;G)
Make rs267607883(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048902
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607883
ebirs267607883
HLIrs267607883
Exacrs267607883
Varsomers267607883
Maprs267607883
PheGenIrs267607883
hapmaprs267607883
1000 genomesrs267607883
hgdprs267607883
ensemblrs267607883
gopubmedrs267607883
geneviewrs267607883
scholarrs267607883
googlers267607883
pharmgkbrs267607883
gwascentralrs267607883
openSNPrs267607883
23andMers267607883
23andMe allrs267607883
SNP Nexus

SNPshotrs267607883
SNPdbers267607883
MSV3drs267607883
GWAS Ctlgrs267607883
Max Magnitude0
ClinVar
Risk rs267607883(G;G)
Alt rs267607883(G;G)
Reference rs267607883(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.37090393A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075469.2, RCV000202242.1,