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rs796051864

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051864(-;-)
Make rs796051864(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position90708875
GeneADGRV1
is asnp
is mentioned by
dbSNPrs796051864
ebirs796051864
HLIrs796051864
Exacrs796051864
Varsomers796051864
Maprs796051864
PheGenIrs796051864
hapmaprs796051864
1000 genomesrs796051864
hgdprs796051864
ensemblrs796051864
gopubmedrs796051864
geneviewrs796051864
scholarrs796051864
googlers796051864
pharmgkbrs796051864
gwascentralrs796051864
openSNPrs796051864
23andMers796051864
23andMe allrs796051864
SNP Nexus

SNPshotrs796051864
SNPdbers796051864
MSV3drs796051864
GWAS Ctlgrs796051864
Max Magnitude0
ClinVar
Risk rs796051864(;)
Alt rs796051864(;)
Reference rs796051864(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.90004692delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007202.4,