Have questions? Visit https://www.reddit.com/r/SNPedia

rs876657695

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657695(-;-)
Make rs876657695(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position90629401
GeneADGRV1
is asnp
is mentioned by
dbSNPrs876657695
ebirs876657695
HLIrs876657695
Exacrs876657695
Varsomers876657695
Maprs876657695
PheGenIrs876657695
hapmaprs876657695
1000 genomesrs876657695
hgdprs876657695
ensemblrs876657695
gopubmedrs876657695
geneviewrs876657695
scholarrs876657695
googlers876657695
pharmgkbrs876657695
gwascentralrs876657695
openSNPrs876657695
23andMers876657695
23andMe allrs876657695
SNP Nexus

SNPshotrs876657695
SNPdbers876657695
MSV3drs876657695
GWAS Ctlgrs876657695
Max Magnitude0
ClinVar
Risk rs876657695(;)
Alt rs876657695(;)
Reference rs876657695(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89925218delC
CLNSRC
CLNACC RCV000221685.1,