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rs587778943

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587778943(-;-)
Make rs587778943(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047535
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778943
ebirs587778943
HLIrs587778943
Exacrs587778943
Varsomers587778943
Maprs587778943
PheGenIrs587778943
hapmaprs587778943
1000 genomesrs587778943
hgdprs587778943
ensemblrs587778943
gopubmedrs587778943
geneviewrs587778943
scholarrs587778943
googlers587778943
pharmgkbrs587778943
gwascentralrs587778943
openSNPrs587778943
23andMers587778943
23andMe allrs587778943
SNP Nexus

SNPshotrs587778943
SNPdbers587778943
MSV3drs587778943
GWAS Ctlgrs587778943
Max Magnitude0
ClinVar
Risk rs587778943(;)
Alt rs587778943(;)
Reference rs587778943(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089026_37089027delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075349.2,