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rs878853272

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853272(C;T)
Make rs878853272(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position1495524
GeneTELO2
is asnp
is mentioned by
dbSNPrs878853272
ebirs878853272
HLIrs878853272
Exacrs878853272
Varsomers878853272
Maprs878853272
PheGenIrs878853272
hapmaprs878853272
1000 genomesrs878853272
hgdprs878853272
ensemblrs878853272
gopubmedrs878853272
geneviewrs878853272
scholarrs878853272
googlers878853272
pharmgkbrs878853272
gwascentralrs878853272
openSNPrs878853272
23andMers878853272
23andMe allrs878853272
SNP Nexus

SNPshotrs878853272
SNPdbers878853272
MSV3drs878853272
GWAS Ctlgrs878853272
Max Magnitude0
ClinVar
Risk rs878853272(T;T)
Alt rs878853272(T;T)
Reference rs878853272(C;C)
Significance Pathogenic
Disease You-Hoover-Fong syndrome
Variation info
Gene TELO2
CLNDBN You-Hoover-Fong syndrome
Reversed 0
HGVS NC_000016.9:g.1545525C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000225207.2,