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rs587781773

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781773(-;-)
Make rs587781773(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position96254994
GeneTMEM127
is asnp
is mentioned by
dbSNPrs587781773
ebirs587781773
HLIrs587781773
Exacrs587781773
Varsomers587781773
Maprs587781773
PheGenIrs587781773
hapmaprs587781773
1000 genomesrs587781773
hgdprs587781773
ensemblrs587781773
gopubmedrs587781773
geneviewrs587781773
scholarrs587781773
googlers587781773
pharmgkbrs587781773
gwascentralrs587781773
openSNPrs587781773
23andMers587781773
23andMe allrs587781773
SNP Nexus

SNPshotrs587781773
SNPdbers587781773
MSV3drs587781773
GWAS Ctlgrs587781773
Max Magnitude0
ClinVar
Risk rs587781773(;)
Alt rs587781773(;)
Reference rs587781773(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TMEM127
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000002.11:g.96920732delA
CLNSRC
CLNACC RCV000130014.2,