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rs878853268

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853268(-;-)
Make rs878853268(-;ATC)
Make rs878853268(ATC;ATC)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position98082956
GeneNANS, TRIM14
is asnp
is mentioned by
dbSNPrs878853268
ebirs878853268
HLIrs878853268
Exacrs878853268
Varsomers878853268
Maprs878853268
PheGenIrs878853268
hapmaprs878853268
1000 genomesrs878853268
hgdprs878853268
ensemblrs878853268
gopubmedrs878853268
geneviewrs878853268
scholarrs878853268
googlers878853268
pharmgkbrs878853268
gwascentralrs878853268
openSNPrs878853268
23andMers878853268
23andMe allrs878853268
SNP Nexus

SNPshotrs878853268
SNPdbers878853268
MSV3drs878853268
GWAS Ctlgrs878853268
Max Magnitude0
ClinVar
Risk rs878853268(CAT;CAT)
Alt rs878853268(CAT;CAT)
Reference rs878853268(;)
Significance Pathogenic
Disease Spondyloepimetaphyseal dysplasia Genevieve type
Variation info
Gene TRIM14 NANS
CLNDBN Spondyloepimetaphyseal dysplasia Genevieve type
Reversed 0
HGVS NC_000009.11:g.100845236_100845238dupATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000224852.1,