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rs587778884

From SNPedia

Orientationplus
Geno Mag Summary
(TGGGGAGA;TGGGGAGA) 0 common in clinvar
Make rs587778884(-;-)
Make rs587778884(-;GGAGATGG)
Make rs587778884(GGAGATGG;GGAGATGG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025669
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778884
ebirs587778884
HLIrs587778884
Exacrs587778884
Varsomers587778884
Maprs587778884
PheGenIrs587778884
hapmaprs587778884
1000 genomesrs587778884
hgdprs587778884
ensemblrs587778884
gopubmedrs587778884
geneviewrs587778884
scholarrs587778884
googlers587778884
pharmgkbrs587778884
gwascentralrs587778884
openSNPrs587778884
23andMers587778884
23andMe allrs587778884
SNP Nexus

SNPshotrs587778884
SNPdbers587778884
MSV3drs587778884
GWAS Ctlgrs587778884
Max Magnitude0
ClinVar
Risk rs587778884(;)
Alt rs587778884(;)
Reference rs587778884(TGGGGAGA;TGGGGAGA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067160_37067167delGGAGATGG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075106.2,