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rs587778933

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778933(A;A)
Make rs587778933(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37040240
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778933
ebirs587778933
HLIrs587778933
Exacrs587778933
Varsomers587778933
Maprs587778933
PheGenIrs587778933
hapmaprs587778933
1000 genomesrs587778933
hgdprs587778933
ensemblrs587778933
gopubmedrs587778933
geneviewrs587778933
scholarrs587778933
googlers587778933
pharmgkbrs587778933
gwascentralrs587778933
openSNPrs587778933
23andMers587778933
23andMe allrs587778933
SNP Nexus

SNPshotrs587778933
SNPdbers587778933
MSV3drs587778933
GWAS Ctlgrs587778933
Max Magnitude0
ClinVar
Risk rs587778933(A;A)
Alt rs587778933(A;A)
Reference rs587778933(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081731G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075276.2,