rs796051867

Orientation

plus

Stabilized

plus

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

Make rs796051867(-;-)

Make rs796051867(-;AA)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

90676123

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs796051867
dbSNP (classic)	rs796051867
ClinGen	rs796051867
ebi	rs796051867
HLI	rs796051867
Exac	rs796051867
Gnomad	rs796051867
Varsome	rs796051867
LitVar	rs796051867
Map	rs796051867
PheGenI	rs796051867
Biobank	rs796051867
1000 genomes	rs796051867
hgdp	rs796051867
ensembl	rs796051867
geneview	rs796051867
scholar	rs796051867
google	rs796051867
pharmgkb	rs796051867
gwascentral	rs796051867
openSNP	rs796051867
23andMe	rs796051867
SNPshot	rs796051867
SNPdbe	rs796051867
MSV3d	rs796051867
GWAS Ctlg	rs796051867

Max Magnitude

0

ClinVar
Risk	rs796051867(-;-)
Alt	rs796051867(-;-)
Reference	Rs796051867(AA;AA)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.89971940_89971941delAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007207.5,