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rs587779019

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779019(-;-)
Make rs587779019(-;GA)
Make rs587779019(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37008884
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779019
ebirs587779019
HLIrs587779019
Exacrs587779019
Varsomers587779019
Maprs587779019
PheGenIrs587779019
hapmaprs587779019
1000 genomesrs587779019
hgdprs587779019
ensemblrs587779019
gopubmedrs587779019
geneviewrs587779019
scholarrs587779019
googlers587779019
pharmgkbrs587779019
gwascentralrs587779019
openSNPrs587779019
23andMers587779019
23andMe allrs587779019
SNP Nexus

SNPshotrs587779019
SNPdbers587779019
MSV3drs587779019
GWAS Ctlgrs587779019
Max Magnitude0
ClinVar
Risk rs587779019(AG;AG)
Alt rs587779019(AG;AG)
Reference rs587779019(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37050375_37050376insGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075742.2,