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rs587779047

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs587779047(-;-)
Make rs587779047(-;AC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37017581
GeneMLH1
is asnp
is mentioned by
dbSNPrs587779047
ebirs587779047
HLIrs587779047
Exacrs587779047
Varsomers587779047
Maprs587779047
PheGenIrs587779047
hapmaprs587779047
1000 genomesrs587779047
hgdprs587779047
ensemblrs587779047
gopubmedrs587779047
geneviewrs587779047
scholarrs587779047
googlers587779047
pharmgkbrs587779047
gwascentralrs587779047
openSNPrs587779047
23andMers587779047
23andMe allrs587779047
SNP Nexus

SNPshotrs587779047
SNPdbers587779047
MSV3drs587779047
GWAS Ctlgrs587779047
Max Magnitude0
ClinVar
Risk rs587779047(;)
Alt rs587779047(;)
Reference rs587779047(AC;AC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059072_37059073delAC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075894.2,