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rs267607717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607717(A;A)
Make rs267607717(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37000954
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607717
ebirs267607717
HLIrs267607717
Exacrs267607717
Varsomers267607717
Maprs267607717
PheGenIrs267607717
hapmaprs267607717
1000 genomesrs267607717
hgdprs267607717
ensemblrs267607717
gopubmedrs267607717
geneviewrs267607717
scholarrs267607717
googlers267607717
pharmgkbrs267607717
gwascentralrs267607717
openSNPrs267607717
23andMers267607717
23andMe allrs267607717
SNP Nexus

SNPshotrs267607717
SNPdbers267607717
MSV3drs267607717
GWAS Ctlgrs267607717
Max Magnitude0
ClinVar
Risk rs267607717(A;A)
Alt rs267607717(A;A)
Reference rs267607717(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042445G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075514.2,