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rs876657694

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657694(A;A)
Make rs876657694(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position90807650
GeneADGRV1
is asnp
is mentioned by
dbSNPrs876657694
ebirs876657694
HLIrs876657694
Exacrs876657694
Varsomers876657694
Maprs876657694
PheGenIrs876657694
hapmaprs876657694
1000 genomesrs876657694
hgdprs876657694
ensemblrs876657694
gopubmedrs876657694
geneviewrs876657694
scholarrs876657694
googlers876657694
pharmgkbrs876657694
gwascentralrs876657694
openSNPrs876657694
23andMers876657694
23andMe allrs876657694
SNP Nexus

SNPshotrs876657694
SNPdbers876657694
MSV3drs876657694
GWAS Ctlgrs876657694
Max Magnitude0
ClinVar
Risk rs876657694(A;A)
Alt rs876657694(A;A)
Reference rs876657694(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90103467G>A
CLNSRC
CLNACC RCV000217974.1,