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rs267607888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607888(C;T)
Make rs267607888(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37049018
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607888
ebirs267607888
HLIrs267607888
Exacrs267607888
Varsomers267607888
Maprs267607888
PheGenIrs267607888
hapmaprs267607888
1000 genomesrs267607888
hgdprs267607888
ensemblrs267607888
gopubmedrs267607888
geneviewrs267607888
scholarrs267607888
googlers267607888
pharmgkbrs267607888
gwascentralrs267607888
openSNPrs267607888
23andMers267607888
23andMe allrs267607888
SNP Nexus

SNPshotrs267607888
SNPdbers267607888
MSV3drs267607888
GWAS Ctlgrs267607888
Max Magnitude0
ClinVar
Risk rs267607888(A,G,T;A,G,T)
Alt rs267607888(A,G,T;A,G,T)
Reference rs267607888(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 1
HGVS NC_000003.11:g.37090509G>A; NC_000003.11:g.37090509G>C; NC_000003.11:g.37090509G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075529.2, RCV000202158.1, RCV000075530.2, RCV000075531.2,