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rs267607879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607879(A;A)
Make rs267607879(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048610
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607879
ebirs267607879
HLIrs267607879
Exacrs267607879
Varsomers267607879
Maprs267607879
PheGenIrs267607879
hapmaprs267607879
1000 genomesrs267607879
hgdprs267607879
ensemblrs267607879
gopubmedrs267607879
geneviewrs267607879
scholarrs267607879
googlers267607879
pharmgkbrs267607879
gwascentralrs267607879
openSNPrs267607879
23andMers267607879
23andMe allrs267607879
SNP Nexus

SNPshotrs267607879
SNPdbers267607879
MSV3drs267607879
GWAS Ctlgrs267607879
Max Magnitude0
ClinVar
Risk rs267607879(A,C,T;A,C,T)
Alt rs267607879(A,C,T;A,C,T)
Reference rs267607879(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090101G>A; NC_000003.11:g.37090101G>C; NC_000003.11:g.37090101G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075455.2, RCV000075456.2, RCV000075457.2,