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rs587778924

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778924(-;-)
Make rs587778924(-;T)
Make rs587778924(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028926
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778924
ebirs587778924
HLIrs587778924
Exacrs587778924
Varsomers587778924
Maprs587778924
PheGenIrs587778924
hapmaprs587778924
1000 genomesrs587778924
hgdprs587778924
ensemblrs587778924
gopubmedrs587778924
geneviewrs587778924
scholarrs587778924
googlers587778924
pharmgkbrs587778924
gwascentralrs587778924
openSNPrs587778924
23andMers587778924
23andMe allrs587778924
SNP Nexus

SNPshotrs587778924
SNPdbers587778924
MSV3drs587778924
GWAS Ctlgrs587778924
Max Magnitude0
ClinVar
Risk rs587778924(T;T)
Alt rs587778924(T;T)
Reference rs587778924(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070417_37070418insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075240.2,