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rs878853348

From SNPedia

Orientationplus
Geno Mag Summary
(CTTC;CTTC) 0 common in clinvar
Make rs878853348(-;-)
Make rs878853348(-;TTCC)
Make rs878853348(TTCC;TTCC)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position90679609
GeneADGRV1
is asnp
is mentioned by
dbSNPrs878853348
ebirs878853348
HLIrs878853348
Exacrs878853348
Varsomers878853348
Maprs878853348
PheGenIrs878853348
hapmaprs878853348
1000 genomesrs878853348
hgdprs878853348
ensemblrs878853348
gopubmedrs878853348
geneviewrs878853348
scholarrs878853348
googlers878853348
pharmgkbrs878853348
gwascentralrs878853348
openSNPrs878853348
23andMers878853348
23andMe allrs878853348
SNP Nexus

SNPshotrs878853348
SNPdbers878853348
MSV3drs878853348
GWAS Ctlgrs878853348
Max Magnitude0
ClinVar
Risk rs878853348(;)
Alt rs878853348(;)
Reference rs878853348(CTTC;CTTC)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene GPR98
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000005.9:g.89975426_89975429delTTCC
CLNSRC
CLNACC RCV000225506.1,