rs121909762

Orientation

plus

Stabilized

plus

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

Make rs121909762(C;T)

Make rs121909762(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

90690991

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs121909762
dbSNP (classic)	rs121909762
ClinGen	rs121909762
ebi	rs121909762
HLI	rs121909762
Exac	rs121909762
Gnomad	rs121909762
Varsome	rs121909762
LitVar	rs121909762
Map	rs121909762
PheGenI	rs121909762
Biobank	rs121909762
1000 genomes	rs121909762
hgdp	rs121909762
ensembl	rs121909762
geneview	rs121909762
scholar	rs121909762
google	rs121909762
pharmgkb	rs121909762
gwascentral	rs121909762
openSNP	rs121909762
23andMe	rs121909762
SNPshot	rs121909762
SNPdbe	rs121909762
MSV3d	rs121909762
GWAS Ctlg	rs121909762

Max Magnitude

0

OMIM	602851
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909762(T;T)
Alt	rs121909762(T;T)
Reference	Rs121909762(C;C)
Significance	Pathogenic
Disease	Usher syndrome Retinitis pigmentosa-deafness syndrome
Variation	info
Gene	GPR98 ADGRV1
CLNDBN	Usher syndrome, type 2C Retinitis pigmentosa-deafness syndrome
Reversed	0
HGVS	NC_000005.9:g.89986808C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007200.5, RCV000397695.1,