Have questions? Visit https://www.reddit.com/r/SNPedia

rs753330544

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753330544(A;A)
Make rs753330544(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position215674595
GeneUSH2A
is asnp
is mentioned by
dbSNPrs753330544
ebirs753330544
HLIrs753330544
Exacrs753330544
Varsomers753330544
Maprs753330544
PheGenIrs753330544
hapmaprs753330544
1000 genomesrs753330544
hgdprs753330544
ensemblrs753330544
gopubmedrs753330544
geneviewrs753330544
scholarrs753330544
googlers753330544
pharmgkbrs753330544
gwascentralrs753330544
openSNPrs753330544
23andMers753330544
23andMe allrs753330544
SNP Nexus

SNPshotrs753330544
SNPdbers753330544
MSV3drs753330544
GWAS Ctlgrs753330544
Max Magnitude0
ClinVar
Risk rs753330544(A;A)
Alt rs753330544(A;A)
Reference rs753330544(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 0
HGVS NC_000001.10:g.215847937G>A
CLNSRC
CLNACC RCV000179630.1,