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rs587778914

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778914(A;C)
Make rs587778914(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36996645
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778914
ebirs587778914
HLIrs587778914
Exacrs587778914
Varsomers587778914
Maprs587778914
PheGenIrs587778914
hapmaprs587778914
1000 genomesrs587778914
hgdprs587778914
ensemblrs587778914
gopubmedrs587778914
geneviewrs587778914
scholarrs587778914
googlers587778914
pharmgkbrs587778914
gwascentralrs587778914
openSNPrs587778914
23andMers587778914
23andMe allrs587778914
SNP Nexus

SNPshotrs587778914
SNPdbers587778914
MSV3drs587778914
GWAS Ctlgrs587778914
Max Magnitude0
ClinVar
Risk rs587778914(C;C)
Alt rs587778914(C;C)
Reference rs587778914(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37038136A>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075213.2,