rs527236131

Orientation

plus

Stabilized

plus

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

Make rs527236131(C;T)

Make rs527236131(T;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

90810996

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs527236131
dbSNP (classic)	rs527236131
ClinGen	rs527236131
ebi	rs527236131
HLI	rs527236131
Exac	rs527236131
Gnomad	rs527236131
Varsome	rs527236131
LitVar	rs527236131
Map	rs527236131
PheGenI	rs527236131
Biobank	rs527236131
1000 genomes	rs527236131
hgdp	rs527236131
ensembl	rs527236131
geneview	rs527236131
scholar	rs527236131
google	rs527236131
pharmgkb	rs527236131
gwascentral	rs527236131
openSNP	rs527236131
23andMe	rs527236131
SNPshot	rs527236131
SNPdbe	rs527236131
MSV3d	rs527236131
GWAS Ctlg	rs527236131

Max Magnitude

0

ClinVar
Risk	rs527236131(T;T)
Alt	rs527236131(T;T)
Reference	Rs527236131(C;C)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	GPR98 ADGRV1
CLNDBN	Usher syndrome, type 2C
Reversed	0
HGVS	NC_000005.9:g.90106813C>T
CLNSRC	ClinVar
CLNACC	RCV000132686.1,