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rs794729203

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729203(A;A)
Make rs794729203(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position215680343
GeneUSH2A
is asnp
is mentioned by
dbSNPrs794729203
ebirs794729203
HLIrs794729203
Exacrs794729203
Varsomers794729203
Maprs794729203
PheGenIrs794729203
hapmaprs794729203
1000 genomesrs794729203
hgdprs794729203
ensemblrs794729203
gopubmedrs794729203
geneviewrs794729203
scholarrs794729203
googlers794729203
pharmgkbrs794729203
gwascentralrs794729203
openSNPrs794729203
23andMers794729203
23andMe allrs794729203
SNP Nexus

SNPshotrs794729203
SNPdbers794729203
MSV3drs794729203
GWAS Ctlgrs794729203
Max Magnitude0
ClinVar
Risk rs794729203(A;A)
Alt rs794729203(A;A)
Reference rs794729203(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.215853685C>T
CLNSRC
CLNACC RCV000184023.1,