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rs267607768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607768(C;C)
Make rs267607768(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37011867
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607768
ebirs267607768
HLIrs267607768
Exacrs267607768
Varsomers267607768
Maprs267607768
PheGenIrs267607768
hapmaprs267607768
1000 genomesrs267607768
hgdprs267607768
ensemblrs267607768
gopubmedrs267607768
geneviewrs267607768
scholarrs267607768
googlers267607768
pharmgkbrs267607768
gwascentralrs267607768
openSNPrs267607768
23andMers267607768
23andMe allrs267607768
SNP Nexus

SNPshotrs267607768
SNPdbers267607768
MSV3drs267607768
GWAS Ctlgrs267607768
Max Magnitude0
ClinVar
Risk rs267607768(A,C;A,C)
Alt rs267607768(A,C;A,C)
Reference rs267607768(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MLH1
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37053358G>A; NC_000003.11:g.37053358G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075774.3, RCV000213543.1, RCV000075775.2,