rs796051864

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs796051864(-;-)

Make rs796051864(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

90708875

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs796051864
dbSNP (classic)	rs796051864
ClinGen	rs796051864
ebi	rs796051864
HLI	rs796051864
Exac	rs796051864
Gnomad	rs796051864
Varsome	rs796051864
LitVar	rs796051864
Map	rs796051864
PheGenI	rs796051864
Biobank	rs796051864
1000 genomes	rs796051864
hgdp	rs796051864
ensembl	rs796051864
geneview	rs796051864
scholar	rs796051864
google	rs796051864
pharmgkb	rs796051864
gwascentral	rs796051864
openSNP	rs796051864
23andMe	rs796051864
SNPshot	rs796051864
SNPdbe	rs796051864
MSV3d	rs796051864
GWAS Ctlg	rs796051864

Max Magnitude

0

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	RCV000007202.5,