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rs876657731

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657731(A;A)
Make rs876657731(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position216073096
GeneLOC102723833, USH2A
is asnp
is mentioned by
dbSNPrs876657731
ebirs876657731
HLIrs876657731
Exacrs876657731
Varsomers876657731
Maprs876657731
PheGenIrs876657731
hapmaprs876657731
1000 genomesrs876657731
hgdprs876657731
ensemblrs876657731
gopubmedrs876657731
geneviewrs876657731
scholarrs876657731
googlers876657731
pharmgkbrs876657731
gwascentralrs876657731
openSNPrs876657731
23andMers876657731
23andMe allrs876657731
SNP Nexus

SNPshotrs876657731
SNPdbers876657731
MSV3drs876657731
GWAS Ctlgrs876657731
Max Magnitude0
ClinVar
Risk rs876657731(A;A)
Alt rs876657731(A;A)
Reference rs876657731(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene LOC102723833 USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216246438C>T
CLNSRC
CLNACC RCV000213465.1,