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rs796051867

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs796051867(-;-)
Make rs796051867(-;AA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position90676123
GeneADGRV1
is asnp
is mentioned by
dbSNPrs796051867
ebirs796051867
HLIrs796051867
Exacrs796051867
Varsomers796051867
Maprs796051867
PheGenIrs796051867
hapmaprs796051867
1000 genomesrs796051867
hgdprs796051867
ensemblrs796051867
gopubmedrs796051867
geneviewrs796051867
scholarrs796051867
googlers796051867
pharmgkbrs796051867
gwascentralrs796051867
openSNPrs796051867
23andMers796051867
23andMe allrs796051867
SNP Nexus

SNPshotrs796051867
SNPdbers796051867
MSV3drs796051867
GWAS Ctlgrs796051867
Max Magnitude0
ClinVar
Risk rs796051867(;)
Alt rs796051867(;)
Reference rs796051867(AA;AA)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene GPR98 ADGRV1
CLNDBN Usher syndrome, type 2C
Reversed 0
HGVS NC_000005.9:g.89971940_89971941delAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007207.4,