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rs876657730

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657730(C;C)
Make rs876657730(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position216418680
GeneUSH2A
is asnp
is mentioned by
dbSNPrs876657730
ebirs876657730
HLIrs876657730
Exacrs876657730
Varsomers876657730
Maprs876657730
PheGenIrs876657730
hapmaprs876657730
1000 genomesrs876657730
hgdprs876657730
ensemblrs876657730
gopubmedrs876657730
geneviewrs876657730
scholarrs876657730
googlers876657730
pharmgkbrs876657730
gwascentralrs876657730
openSNPrs876657730
23andMers876657730
23andMe allrs876657730
SNP Nexus

SNPshotrs876657730
SNPdbers876657730
MSV3drs876657730
GWAS Ctlgrs876657730
Max Magnitude0
ClinVar
Risk rs876657730(C;C)
Alt rs876657730(C;C)
Reference rs876657730(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216592022C>G
CLNSRC
CLNACC RCV000220465.1,