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rs587778928

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587778928(-;-)
Make rs587778928(-;GT)
Make rs587778928(GT;GT)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040199
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778928
ebirs587778928
HLIrs587778928
Exacrs587778928
Varsomers587778928
Maprs587778928
PheGenIrs587778928
hapmaprs587778928
1000 genomesrs587778928
hgdprs587778928
ensemblrs587778928
gopubmedrs587778928
geneviewrs587778928
scholarrs587778928
googlers587778928
pharmgkbrs587778928
gwascentralrs587778928
openSNPrs587778928
23andMers587778928
23andMe allrs587778928
SNP Nexus

SNPshotrs587778928
SNPdbers587778928
MSV3drs587778928
GWAS Ctlgrs587778928
Max Magnitude0
ClinVar
Risk rs587778928(;)
Alt rs587778928(;)
Reference rs587778928(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081690_37081691delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075269.2,