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rs587778899

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778899(-;-)
Make rs587778899(-;GTCAGCC)
Make rs587778899(GTCAGCC;GTCAGCC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025821
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778899
ebirs587778899
HLIrs587778899
Exacrs587778899
Varsomers587778899
Maprs587778899
PheGenIrs587778899
hapmaprs587778899
1000 genomesrs587778899
hgdprs587778899
ensemblrs587778899
gopubmedrs587778899
geneviewrs587778899
scholarrs587778899
googlers587778899
pharmgkbrs587778899
gwascentralrs587778899
openSNPrs587778899
23andMers587778899
23andMe allrs587778899
SNP Nexus

SNPshotrs587778899
SNPdbers587778899
MSV3drs587778899
GWAS Ctlgrs587778899
Max Magnitude0
ClinVar
Risk rs587778899(GTCAGCC;GTCAGCC)
Alt rs587778899(GTCAGCC;GTCAGCC)
Reference rs587778899(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067306_37067312dupGTCAGCC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075153.2,