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rs587778925

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778925(-;-)
Make rs587778925(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028926
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778925
ebirs587778925
HLIrs587778925
Exacrs587778925
Varsomers587778925
Maprs587778925
PheGenIrs587778925
hapmaprs587778925
1000 genomesrs587778925
hgdprs587778925
ensemblrs587778925
gopubmedrs587778925
geneviewrs587778925
scholarrs587778925
googlers587778925
pharmgkbrs587778925
gwascentralrs587778925
openSNPrs587778925
23andMers587778925
23andMe allrs587778925
SNP Nexus

SNPshotrs587778925
SNPdbers587778925
MSV3drs587778925
GWAS Ctlgrs587778925
Max Magnitude0
ClinVar
Risk rs587778925(;)
Alt rs587778925(;)
Reference rs587778925(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070417delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075241.2,