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rs202175091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202175091(A;A)
Make rs202175091(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position215782070
GeneUSH2A
is asnp
is mentioned by
dbSNPrs202175091
ebirs202175091
HLIrs202175091
Exacrs202175091
Varsomers202175091
Maprs202175091
PheGenIrs202175091
hapmaprs202175091
1000 genomesrs202175091
hgdprs202175091
ensemblrs202175091
gopubmedrs202175091
geneviewrs202175091
scholarrs202175091
googlers202175091
pharmgkbrs202175091
gwascentralrs202175091
openSNPrs202175091
23andMers202175091
23andMe allrs202175091
SNP Nexus

SNPshotrs202175091
SNPdbers202175091
MSV3drs202175091
GWAS Ctlgrs202175091
Max Magnitude0
ClinVar
Risk rs202175091(A;A)
Alt rs202175091(A;A)
Reference rs202175091(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 0
HGVS NC_000001.10:g.215955412G>A
CLNSRC ClinVar
CLNACC RCV000041676.2,