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rs587778930

From SNPedia

Orientationplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587778930(-;-)
Make rs587778930(-;TTC)
Make rs587778930(TTC;TTC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040215
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778930
ebirs587778930
HLIrs587778930
Exacrs587778930
Varsomers587778930
Maprs587778930
PheGenIrs587778930
hapmaprs587778930
1000 genomesrs587778930
hgdprs587778930
ensemblrs587778930
gopubmedrs587778930
geneviewrs587778930
scholarrs587778930
googlers587778930
pharmgkbrs587778930
gwascentralrs587778930
openSNPrs587778930
23andMers587778930
23andMe allrs587778930
SNP Nexus

SNPshotrs587778930
SNPdbers587778930
MSV3drs587778930
GWAS Ctlgrs587778930
Max Magnitude0
ClinVar
Risk rs587778930(;)
Alt rs587778930(;)
Reference rs587778930(CTT;CTT)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37081706_37081708delTTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075272.2, RCV000130099.2,