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rs587778987

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587778987(-;-)
Make rs587778987(-;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37050563
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778987
ebirs587778987
HLIrs587778987
Exacrs587778987
Varsomers587778987
Maprs587778987
PheGenIrs587778987
hapmaprs587778987
1000 genomesrs587778987
hgdprs587778987
ensemblrs587778987
gopubmedrs587778987
geneviewrs587778987
scholarrs587778987
googlers587778987
pharmgkbrs587778987
gwascentralrs587778987
openSNPrs587778987
23andMers587778987
23andMe allrs587778987
SNP Nexus

SNPshotrs587778987
SNPdbers587778987
MSV3drs587778987
GWAS Ctlgrs587778987
Max Magnitude0
ClinVar
Risk rs587778987(;)
Alt rs587778987(;)
Reference rs587778987(CA;CA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092054_37092055delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075570.2,