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rs587781554

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781554(-;-)
Make rs587781554(-;A)
Make rs587781554(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37020396
GeneMLH1
is asnp
is mentioned by
dbSNPrs587781554
ebirs587781554
HLIrs587781554
Exacrs587781554
Varsomers587781554
Maprs587781554
PheGenIrs587781554
hapmaprs587781554
1000 genomesrs587781554
hgdprs587781554
ensemblrs587781554
gopubmedrs587781554
geneviewrs587781554
scholarrs587781554
googlers587781554
pharmgkbrs587781554
gwascentralrs587781554
openSNPrs587781554
23andMers587781554
23andMe allrs587781554
SNP Nexus

SNPshotrs587781554
SNPdbers587781554
MSV3drs587781554
GWAS Ctlgrs587781554
Max Magnitude0
ClinVar
Risk rs587781554(A;A)
Alt rs587781554(A;A)
Reference rs587781554(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061887dupA
CLNSRC
CLNACC RCV000129570.2, RCV000168452.1,