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rs878853273

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853273(A;A)
Make rs878853273(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position1505602
GeneTELO2
is asnp
is mentioned by
dbSNPrs878853273
ebirs878853273
HLIrs878853273
Exacrs878853273
Varsomers878853273
Maprs878853273
PheGenIrs878853273
hapmaprs878853273
1000 genomesrs878853273
hgdprs878853273
ensemblrs878853273
gopubmedrs878853273
geneviewrs878853273
scholarrs878853273
googlers878853273
pharmgkbrs878853273
gwascentralrs878853273
openSNPrs878853273
23andMers878853273
23andMe allrs878853273
SNP Nexus

SNPshotrs878853273
SNPdbers878853273
MSV3drs878853273
GWAS Ctlgrs878853273
Max Magnitude0
ClinVar
Risk rs878853273(A;A)
Alt rs878853273(A;A)
Reference rs878853273(G;G)
Significance Pathogenic
Disease You-Hoover-Fong syndrome
Variation info
Gene TELO2
CLNDBN You-Hoover-Fong syndrome
Reversed 0
HGVS NC_000016.9:g.1555603G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000225207.2,