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rs878853233

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853233(-;-)
Make rs878853233(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position215813790
GeneUSH2A
is asnp
is mentioned by
dbSNPrs878853233
ebirs878853233
HLIrs878853233
Exacrs878853233
Varsomers878853233
Maprs878853233
PheGenIrs878853233
hapmaprs878853233
1000 genomesrs878853233
hgdprs878853233
ensemblrs878853233
gopubmedrs878853233
geneviewrs878853233
scholarrs878853233
googlers878853233
pharmgkbrs878853233
gwascentralrs878853233
openSNPrs878853233
23andMers878853233
23andMe allrs878853233
SNP Nexus

SNPshotrs878853233
SNPdbers878853233
MSV3drs878853233
GWAS Ctlgrs878853233
Max Magnitude0
ClinVar
Risk rs878853233(;)
Alt rs878853233(;)
Reference rs878853233(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene USH2A
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000001.10:g.215987132delC
CLNSRC
CLNACC RCV000225050.1,