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rs587779050

From SNPedia

Orientationplus
Geno Mag Summary
(AGGT;AGGT) 0 common in clinvar
Make rs587779050(-;-)
Make rs587779050(-;GGTA)
Make rs587779050(GGTA;GGTA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017599
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779050
ebirs587779050
HLIrs587779050
Exacrs587779050
Varsomers587779050
Maprs587779050
PheGenIrs587779050
hapmaprs587779050
1000 genomesrs587779050
hgdprs587779050
ensemblrs587779050
gopubmedrs587779050
geneviewrs587779050
scholarrs587779050
googlers587779050
pharmgkbrs587779050
gwascentralrs587779050
openSNPrs587779050
23andMers587779050
23andMe allrs587779050
SNP Nexus

SNPshotrs587779050
SNPdbers587779050
MSV3drs587779050
GWAS Ctlgrs587779050
Max Magnitude0
ClinVar
Risk rs587779050(;)
Alt rs587779050(;)
Reference rs587779050(AGGT;AGGT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059090_37059093delGGTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075910.2,