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rs878853410

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853410(-;-)
Make rs878853410(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position216321969
GeneUSH2A
is asnp
is mentioned by
dbSNPrs878853410
ebirs878853410
HLIrs878853410
Exacrs878853410
Varsomers878853410
Maprs878853410
PheGenIrs878853410
hapmaprs878853410
1000 genomesrs878853410
hgdprs878853410
ensemblrs878853410
gopubmedrs878853410
geneviewrs878853410
scholarrs878853410
googlers878853410
pharmgkbrs878853410
gwascentralrs878853410
openSNPrs878853410
23andMers878853410
23andMe allrs878853410
SNP Nexus

SNPshotrs878853410
SNPdbers878853410
MSV3drs878853410
GWAS Ctlgrs878853410
Max Magnitude0
ClinVar
Risk rs878853410(;)
Alt rs878853410(;)
Reference rs878853410(T;T)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene USH2A
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.216495311delA
CLNSRC
CLNACC RCV000225369.1,