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rs587781892

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781892(-;-)
Make rs587781892(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37025999
GeneMLH1
is asnp
is mentioned by
dbSNPrs587781892
ebirs587781892
HLIrs587781892
Exacrs587781892
Varsomers587781892
Maprs587781892
PheGenIrs587781892
hapmaprs587781892
1000 genomesrs587781892
hgdprs587781892
ensemblrs587781892
gopubmedrs587781892
geneviewrs587781892
scholarrs587781892
googlers587781892
pharmgkbrs587781892
gwascentralrs587781892
openSNPrs587781892
23andMers587781892
23andMe allrs587781892
SNP Nexus

SNPshotrs587781892
SNPdbers587781892
MSV3drs587781892
GWAS Ctlgrs587781892
Max Magnitude0
ClinVar
Risk rs587781892(;)
Alt rs587781892(;)
Reference rs587781892(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067490delC
CLNSRC
CLNACC RCV000130228.2,