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rs587779006

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs587779006(-;-)
Make rs587779006(-;TG)
Make rs587779006(TG;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37004466
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779006
ebirs587779006
HLIrs587779006
Exacrs587779006
Varsomers587779006
Maprs587779006
PheGenIrs587779006
hapmaprs587779006
1000 genomesrs587779006
hgdprs587779006
ensemblrs587779006
gopubmedrs587779006
geneviewrs587779006
scholarrs587779006
googlers587779006
pharmgkbrs587779006
gwascentralrs587779006
openSNPrs587779006
23andMers587779006
23andMe allrs587779006
SNP Nexus

SNPshotrs587779006
SNPdbers587779006
MSV3drs587779006
GWAS Ctlgrs587779006
Max Magnitude0
ClinVar
Risk rs587779006(;)
Alt rs587779006(;)
Reference rs587779006(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37045957_37045958delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075670.2,