rs527236132

Orientation

plus

Stabilized

plus

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

Make rs527236132(G;T)

Make rs527236132(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

90774304

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs527236132
dbSNP (classic)	rs527236132
ClinGen	rs527236132
ebi	rs527236132
HLI	rs527236132
Exac	rs527236132
Gnomad	rs527236132
Varsome	rs527236132
LitVar	rs527236132
Map	rs527236132
PheGenI	rs527236132
Biobank	rs527236132
1000 genomes	rs527236132
hgdp	rs527236132
ensembl	rs527236132
geneview	rs527236132
scholar	rs527236132
google	rs527236132
pharmgkb	rs527236132
gwascentral	rs527236132
openSNP	rs527236132
23andMe	rs527236132
SNPshot	rs527236132
SNPdbe	rs527236132
MSV3d	rs527236132
GWAS Ctlg	rs527236132

Max Magnitude

0

ClinVar
Risk	rs527236132(T;T)
Alt	rs527236132(T;T)
Reference	Rs527236132(G;G)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.90070121G>T
CLNSRC	ClinVar
CLNACC	RCV000132685.1,