rs1060499795

Orientation

plus

Stabilized

plus

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

Make rs1060499795(A;A)

Make rs1060499795(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

90728933

Gene	ADGRV1, LOC105379077

is a	snp
is	mentioned by
dbSNP	rs1060499795
dbSNP (classic)	rs1060499795
ClinGen	rs1060499795
ebi	rs1060499795
HLI	rs1060499795
Exac	rs1060499795
Gnomad	rs1060499795
Varsome	rs1060499795
LitVar	rs1060499795
Map	rs1060499795
PheGenI	rs1060499795
Biobank	rs1060499795
1000 genomes	rs1060499795
hgdp	rs1060499795
ensembl	rs1060499795
geneview	rs1060499795
scholar	rs1060499795
google	rs1060499795
pharmgkb	rs1060499795
gwascentral	rs1060499795
openSNP	rs1060499795
23andMe	rs1060499795
SNPshot	rs1060499795
SNPdbe	rs1060499795
MSV3d	rs1060499795
GWAS Ctlg	rs1060499795

Max Magnitude

0

ClinVar
Risk	rs1060499795(A;A)
Alt	rs1060499795(A;A)
Reference	Rs1060499795(G;G)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.90024750G>A
CLNSRC
CLNACC	RCV000454263.1,