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rs267607895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607895(C;C)
Make rs267607895(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050647
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607895
ebirs267607895
HLIrs267607895
Exacrs267607895
Varsomers267607895
Maprs267607895
PheGenIrs267607895
hapmaprs267607895
1000 genomesrs267607895
hgdprs267607895
ensemblrs267607895
gopubmedrs267607895
geneviewrs267607895
scholarrs267607895
googlers267607895
pharmgkbrs267607895
gwascentralrs267607895
openSNPrs267607895
23andMers267607895
23andMe allrs267607895
SNP Nexus

SNPshotrs267607895
SNPdbers267607895
MSV3drs267607895
GWAS Ctlgrs267607895
Max Magnitude0
ClinVar
Risk rs267607895(C;C)
Alt rs267607895(C;C)
Reference rs267607895(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092138G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075592.2,