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rs267607795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607795(C;C)
Make rs267607795(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017505
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607795
ebirs267607795
HLIrs267607795
Exacrs267607795
Varsomers267607795
Maprs267607795
PheGenIrs267607795
hapmaprs267607795
1000 genomesrs267607795
hgdprs267607795
ensemblrs267607795
gopubmedrs267607795
geneviewrs267607795
scholarrs267607795
googlers267607795
pharmgkbrs267607795
gwascentralrs267607795
openSNPrs267607795
23andMers267607795
23andMe allrs267607795
SNP Nexus

SNPshotrs267607795
SNPdbers267607795
MSV3drs267607795
GWAS Ctlgrs267607795
Max Magnitude0
ClinVar
Risk rs267607795(A,C,T;A,C,T)
Alt rs267607795(A,C,T;A,C,T)
Reference rs267607795(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37058996G>A; NC_000003.11:g.37058996G>C; NC_000003.11:g.37058996G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000168716.1, RCV000075860.2, RCV000075861.2,