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rs587778915

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778915(-;-)
Make rs587778915(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37028823
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778915
ebirs587778915
HLIrs587778915
Exacrs587778915
Varsomers587778915
Maprs587778915
PheGenIrs587778915
hapmaprs587778915
1000 genomesrs587778915
hgdprs587778915
ensemblrs587778915
gopubmedrs587778915
geneviewrs587778915
scholarrs587778915
googlers587778915
pharmgkbrs587778915
gwascentralrs587778915
openSNPrs587778915
23andMers587778915
23andMe allrs587778915
SNP Nexus

SNPshotrs587778915
SNPdbers587778915
MSV3drs587778915
GWAS Ctlgrs587778915
Max Magnitude0
ClinVar
Risk rs587778915(;)
Alt rs587778915(;)
Reference rs587778915(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070314delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075214.2,