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rs267607719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs267607719(-;-)
Make rs267607719(-;GT)
ReferenceGRCh38 38.1/141
Chromosome3
Position36996710
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607719
ebirs267607719
HLIrs267607719
Exacrs267607719
Varsomers267607719
Maprs267607719
PheGenIrs267607719
hapmaprs267607719
1000 genomesrs267607719
hgdprs267607719
ensemblrs267607719
gopubmedrs267607719
geneviewrs267607719
scholarrs267607719
googlers267607719
pharmgkbrs267607719
gwascentralrs267607719
openSNPrs267607719
23andMers267607719
23andMe allrs267607719
SNP Nexus

SNPshotrs267607719
SNPdbers267607719
MSV3drs267607719
GWAS Ctlgrs267607719
Max Magnitude0
ClinVar
Risk rs267607719(;)
Alt rs267607719(;)
Reference rs267607719(GT;GT)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038201_37038202delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075507.2,