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rs587778887

From SNPedia

Orientationplus
Geno Mag Summary
(GTC;GTC) 0 common in clinvar
Make rs587778887(A;A)
Make rs587778887(A;GTC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025730
GeneMLH1
is asnp
is mentioned by
dbSNPrs587778887
ebirs587778887
HLIrs587778887
Exacrs587778887
Varsomers587778887
Maprs587778887
PheGenIrs587778887
hapmaprs587778887
1000 genomesrs587778887
hgdprs587778887
ensemblrs587778887
gopubmedrs587778887
geneviewrs587778887
scholarrs587778887
googlers587778887
pharmgkbrs587778887
gwascentralrs587778887
openSNPrs587778887
23andMers587778887
23andMe allrs587778887
SNP Nexus

SNPshotrs587778887
SNPdbers587778887
MSV3drs587778887
GWAS Ctlgrs587778887
Max Magnitude0
ClinVar
Risk rs587778887(A;A)
Alt rs587778887(A;A)
Reference rs587778887(GTC;GTC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37067221_37067223delGTCinsA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075117.2,