rs1060499796

Orientation

plus

Stabilized

plus

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

Make rs1060499796(A;A)

Make rs1060499796(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

90644869

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs1060499796
dbSNP (classic)	rs1060499796
ClinGen	rs1060499796
ebi	rs1060499796
HLI	rs1060499796
Exac	rs1060499796
Gnomad	rs1060499796
Varsome	rs1060499796
LitVar	rs1060499796
Map	rs1060499796
PheGenI	rs1060499796
Biobank	rs1060499796
1000 genomes	rs1060499796
hgdp	rs1060499796
ensembl	rs1060499796
geneview	rs1060499796
scholar	rs1060499796
google	rs1060499796
pharmgkb	rs1060499796
gwascentral	rs1060499796
openSNP	rs1060499796
23andMe	rs1060499796
SNPshot	rs1060499796
SNPdbe	rs1060499796
MSV3d	rs1060499796
GWAS Ctlg	rs1060499796

Max Magnitude

0

ClinVar
Risk	rs1060499796(A;A)
Alt	rs1060499796(A;A)
Reference	Rs1060499796(G;G)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.89940686G>A
CLNSRC
CLNACC	RCV000454318.1,