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rs587778885

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778885(-;-)
Make rs587778885(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025670
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778885
ebirs587778885
HLIrs587778885
Exacrs587778885
Varsomers587778885
Maprs587778885
PheGenIrs587778885
hapmaprs587778885
1000 genomesrs587778885
hgdprs587778885
ensemblrs587778885
gopubmedrs587778885
geneviewrs587778885
scholarrs587778885
googlers587778885
pharmgkbrs587778885
gwascentralrs587778885
openSNPrs587778885
23andMers587778885
23andMe allrs587778885
SNP Nexus

SNPshotrs587778885
SNPdbers587778885
MSV3drs587778885
GWAS Ctlgrs587778885
Max Magnitude0
ClinVar
Risk rs587778885(;)
Alt rs587778885(;)
Reference rs587778885(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067161delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075107.2,