rs886039893

Orientation

plus

Stabilized

plus

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

Make rs886039893(G;T)

Make rs886039893(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

90694362

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs886039893
dbSNP (classic)	rs886039893
ClinGen	rs886039893
ebi	rs886039893
HLI	rs886039893
Exac	rs886039893
Gnomad	rs886039893
Varsome	rs886039893
LitVar	rs886039893
Map	rs886039893
PheGenI	rs886039893
Biobank	rs886039893
1000 genomes	rs886039893
hgdp	rs886039893
ensembl	rs886039893
geneview	rs886039893
scholar	rs886039893
google	rs886039893
pharmgkb	rs886039893
gwascentral	rs886039893
openSNP	rs886039893
23andMe	rs886039893
SNPshot	rs886039893
SNPdbe	rs886039893
MSV3d	rs886039893
GWAS Ctlg	rs886039893

Max Magnitude

0

ClinVar
Risk	rs886039893(T;T)
Alt	rs886039893(T;T)
Reference	Rs886039893(G;G)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	GPR98 ADGRV1
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.89990179G>T
CLNSRC
CLNACC	RCV000256377.1,