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rs267607903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607903(-;-)
Make rs267607903(-;AACA)
Make rs267607903(AACA;AACA)
ReferenceGRCh38 38.1/141
Chromosome3
Position37050580
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607903
ebirs267607903
HLIrs267607903
Exacrs267607903
Varsomers267607903
Maprs267607903
PheGenIrs267607903
hapmaprs267607903
1000 genomesrs267607903
hgdprs267607903
ensemblrs267607903
gopubmedrs267607903
geneviewrs267607903
scholarrs267607903
googlers267607903
pharmgkbrs267607903
gwascentralrs267607903
openSNPrs267607903
23andMers267607903
23andMe allrs267607903
SNP Nexus

SNPshotrs267607903
SNPdbers267607903
MSV3drs267607903
GWAS Ctlgrs267607903
Max Magnitude0
ClinVar
Risk rs267607903(AAAC;AAAC)
Alt rs267607903(AAAC;AAAC)
Reference rs267607903(;)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37092068_37092071dupAACA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075574.2, RCV000202055.1,