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rs587778950

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778950(-;-)
Make rs587778950(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047653
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778950
ebirs587778950
HLIrs587778950
Exacrs587778950
Varsomers587778950
Maprs587778950
PheGenIrs587778950
hapmaprs587778950
1000 genomesrs587778950
hgdprs587778950
ensemblrs587778950
gopubmedrs587778950
geneviewrs587778950
scholarrs587778950
googlers587778950
pharmgkbrs587778950
gwascentralrs587778950
openSNPrs587778950
23andMers587778950
23andMe allrs587778950
SNP Nexus

SNPshotrs587778950
SNPdbers587778950
MSV3drs587778950
GWAS Ctlgrs587778950
Max Magnitude0
ClinVar
Risk rs587778950(;)
Alt rs587778950(;)
Reference rs587778950(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089144delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075391.2,