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rs878852981

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878852981(C;C)
Make rs878852981(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position98078306
GeneNANS
is asnp
is mentioned by
dbSNPrs878852981
ebirs878852981
HLIrs878852981
Exacrs878852981
Varsomers878852981
Maprs878852981
PheGenIrs878852981
hapmaprs878852981
1000 genomesrs878852981
hgdprs878852981
ensemblrs878852981
gopubmedrs878852981
geneviewrs878852981
scholarrs878852981
googlers878852981
pharmgkbrs878852981
gwascentralrs878852981
openSNPrs878852981
23andMers878852981
23andMe allrs878852981
SNP Nexus

SNPshotrs878852981
SNPdbers878852981
MSV3drs878852981
GWAS Ctlgrs878852981
Max Magnitude0
ClinVar
Risk rs878852981(C;C)
Alt rs878852981(C;C)
Reference rs878852981(T;T)
Significance Pathogenic
Disease Spondyloepimetaphyseal dysplasia Genevieve type
Variation info
Gene TRIM14 NANS
CLNDBN Spondyloepimetaphyseal dysplasia Genevieve type
Reversed 0
HGVS NC_000009.11:g.100840588T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000224249.1,