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rs876657732

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657732(-;-)
Make rs876657732(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position215998905
GeneUSH2A
is asnp
is mentioned by
dbSNPrs876657732
ebirs876657732
HLIrs876657732
Exacrs876657732
Varsomers876657732
Maprs876657732
PheGenIrs876657732
hapmaprs876657732
1000 genomesrs876657732
hgdprs876657732
ensemblrs876657732
gopubmedrs876657732
geneviewrs876657732
scholarrs876657732
googlers876657732
pharmgkbrs876657732
gwascentralrs876657732
openSNPrs876657732
23andMers876657732
23andMe allrs876657732
SNP Nexus

SNPshotrs876657732
SNPdbers876657732
MSV3drs876657732
GWAS Ctlgrs876657732
Max Magnitude0
ClinVar
Risk rs876657732(;)
Alt rs876657732(;)
Reference rs876657732(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216172247delT
CLNSRC
CLNACC RCV000217100.1,