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rs878853385

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853385(-;-)
Make rs878853385(-;C)
Make rs878853385(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position88431201
GeneSPATA7
is asnp
is mentioned by
dbSNPrs878853385
ebirs878853385
HLIrs878853385
Exacrs878853385
Varsomers878853385
Maprs878853385
PheGenIrs878853385
hapmaprs878853385
1000 genomesrs878853385
hgdprs878853385
ensemblrs878853385
gopubmedrs878853385
geneviewrs878853385
scholarrs878853385
googlers878853385
pharmgkbrs878853385
gwascentralrs878853385
openSNPrs878853385
23andMers878853385
23andMe allrs878853385
SNP Nexus

SNPshotrs878853385
SNPdbers878853385
MSV3drs878853385
GWAS Ctlgrs878853385
Max Magnitude0
ClinVar
Risk rs878853385(C;C)
Alt rs878853385(C;C)
Reference rs878853385(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene SPATA7
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000014.8:g.88897545dupC
CLNSRC
CLNACC RCV000225504.1,