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rs779791079

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs779791079(-;-)
Make rs779791079(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position215728220
GeneUSH2A
is asnp
is mentioned by
dbSNPrs779791079
ebirs779791079
HLIrs779791079
Exacrs779791079
Varsomers779791079
Maprs779791079
PheGenIrs779791079
hapmaprs779791079
1000 genomesrs779791079
hgdprs779791079
ensemblrs779791079
gopubmedrs779791079
geneviewrs779791079
scholarrs779791079
googlers779791079
pharmgkbrs779791079
gwascentralrs779791079
openSNPrs779791079
23andMers779791079
23andMe allrs779791079
SNP Nexus

SNPshotrs779791079
SNPdbers779791079
MSV3drs779791079
GWAS Ctlgrs779791079
Max Magnitude0
ClinVar
Risk rs779791079(;)
Alt rs779791079(;)
Reference rs779791079(TG;TG)
Significance Pathogenic
Disease Usher syndrome Retinitis pigmentosa 39
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A Retinitis pigmentosa 39
Reversed 0
HGVS NC_000001.10:g.215901562_215901563delTG
CLNSRC
CLNACC RCV000179599.1, RCV000179600.1,