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rs267607715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607715(-;-)
Make rs267607715(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996697
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607715
ebirs267607715
HLIrs267607715
Exacrs267607715
Varsomers267607715
Maprs267607715
PheGenIrs267607715
hapmaprs267607715
1000 genomesrs267607715
hgdprs267607715
ensemblrs267607715
gopubmedrs267607715
geneviewrs267607715
scholarrs267607715
googlers267607715
pharmgkbrs267607715
gwascentralrs267607715
openSNPrs267607715
23andMers267607715
23andMe allrs267607715
SNP Nexus

SNPshotrs267607715
SNPdbers267607715
MSV3drs267607715
GWAS Ctlgrs267607715
Max Magnitude0
ClinVar
Risk rs267607715(;)
Alt rs267607715(;)
Reference rs267607715(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038188delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075438.2,