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rs267607819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607819(C;T)
Make rs267607819(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025636
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607819
ebirs267607819
HLIrs267607819
Exacrs267607819
Varsomers267607819
Maprs267607819
PheGenIrs267607819
hapmaprs267607819
1000 genomesrs267607819
hgdprs267607819
ensemblrs267607819
gopubmedrs267607819
geneviewrs267607819
scholarrs267607819
googlers267607819
pharmgkbrs267607819
gwascentralrs267607819
openSNPrs267607819
23andMers267607819
23andMe allrs267607819
SNP Nexus

SNPshotrs267607819
SNPdbers267607819
MSV3drs267607819
GWAS Ctlgrs267607819
Max Magnitude0
ClinVar
Risk rs267607819(G,T;G,T)
Alt rs267607819(G,T;G,T)
Reference rs267607819(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.37067127G>A
CLNSRC HGMD International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075088.2, RCV000153506.4,