Have questions? Visit https://www.reddit.com/r/SNPedia

rs11541859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11541859(C;C)
Make rs11541859(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37001012
GeneMLH1
is asnp
is mentioned by
dbSNPrs11541859
ebirs11541859
HLIrs11541859
Exacrs11541859
Varsomers11541859
Maprs11541859
PheGenIrs11541859
hapmaprs11541859
1000 genomesrs11541859
hgdprs11541859
ensemblrs11541859
gopubmedrs11541859
geneviewrs11541859
scholarrs11541859
googlers11541859
pharmgkbrs11541859
gwascentralrs11541859
openSNPrs11541859
23andMers11541859
23andMe allrs11541859
SNP Nexus

SNPshotrs11541859
SNPdbers11541859
MSV3drs11541859
GWAS Ctlgrs11541859
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs11541859(C,T;C,T)
Alt rs11541859(C,T;C,T)
Reference rs11541859(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37042503G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075610.2,