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rs587778909

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587778909(-;-)
Make rs587778909(-;GA)
Make rs587778909(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025978
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778909
ebirs587778909
HLIrs587778909
Exacrs587778909
Varsomers587778909
Maprs587778909
PheGenIrs587778909
hapmaprs587778909
1000 genomesrs587778909
hgdprs587778909
ensemblrs587778909
gopubmedrs587778909
geneviewrs587778909
scholarrs587778909
googlers587778909
pharmgkbrs587778909
gwascentralrs587778909
openSNPrs587778909
23andMers587778909
23andMe allrs587778909
SNP Nexus

SNPshotrs587778909
SNPdbers587778909
MSV3drs587778909
GWAS Ctlgrs587778909
Max Magnitude0
ClinVar
Risk rs587778909(;)
Alt rs587778909(;)
Reference rs587778909(AG;AG)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067469_37067470delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075185.2, RCV000165092.1,