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rs587779014

From SNPedia

Orientationplus
Geno Mag Summary
(TGAA;TGAA) 0 common in clinvar
Make rs587779014(-;-)
Make rs587779014(-;TGAA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37007014
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779014
ebirs587779014
HLIrs587779014
Exacrs587779014
Varsomers587779014
Maprs587779014
PheGenIrs587779014
hapmaprs587779014
1000 genomesrs587779014
hgdprs587779014
ensemblrs587779014
gopubmedrs587779014
geneviewrs587779014
scholarrs587779014
googlers587779014
pharmgkbrs587779014
gwascentralrs587779014
openSNPrs587779014
23andMers587779014
23andMe allrs587779014
SNP Nexus

SNPshotrs587779014
SNPdbers587779014
MSV3drs587779014
GWAS Ctlgrs587779014
Max Magnitude0
ClinVar
Risk rs587779014(;)
Alt rs587779014(;)
Reference rs587779014(TGAA;TGAA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37048505_37048508delTGAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075702.2,