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rs587779018

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779018(-;-)
Make rs587779018(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37008857
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779018
ebirs587779018
HLIrs587779018
Exacrs587779018
Varsomers587779018
Maprs587779018
PheGenIrs587779018
hapmaprs587779018
1000 genomesrs587779018
hgdprs587779018
ensemblrs587779018
gopubmedrs587779018
geneviewrs587779018
scholarrs587779018
googlers587779018
pharmgkbrs587779018
gwascentralrs587779018
openSNPrs587779018
23andMers587779018
23andMe allrs587779018
SNP Nexus

SNPshotrs587779018
SNPdbers587779018
MSV3drs587779018
GWAS Ctlgrs587779018
Max Magnitude0
ClinVar
Risk rs587779018(;)
Alt rs587779018(;)
Reference rs587779018(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050348delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075736.2,