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rs587778966

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778966(-;-)
Make rs587778966(-;C)
Make rs587778966(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996700
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778966
ebirs587778966
HLIrs587778966
Exacrs587778966
Varsomers587778966
Maprs587778966
PheGenIrs587778966
hapmaprs587778966
1000 genomesrs587778966
hgdprs587778966
ensemblrs587778966
gopubmedrs587778966
geneviewrs587778966
scholarrs587778966
googlers587778966
pharmgkbrs587778966
gwascentralrs587778966
openSNPrs587778966
23andMers587778966
23andMe allrs587778966
SNP Nexus

SNPshotrs587778966
SNPdbers587778966
MSV3drs587778966
GWAS Ctlgrs587778966
Max Magnitude0
ClinVar
Risk rs587778966(C;C)
Alt rs587778966(C;C)
Reference rs587778966(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038191dupC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075464.2,