rs876657732

Orientation

minus

Stabilized

minus

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

Make rs876657732(-;-)

Make rs876657732(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

215998905

Gene

USH2A

is a	snp
is	mentioned by
dbSNP	rs876657732
dbSNP (classic)	rs876657732
ClinGen	rs876657732
ebi	rs876657732
HLI	rs876657732
Exac	rs876657732
Gnomad	rs876657732
Varsome	rs876657732
LitVar	rs876657732
Map	rs876657732
PheGenI	rs876657732
Biobank	rs876657732
1000 genomes	rs876657732
hgdp	rs876657732
ensembl	rs876657732
geneview	rs876657732
scholar	rs876657732
google	rs876657732
pharmgkb	rs876657732
gwascentral	rs876657732
openSNP	rs876657732
23andMe	rs876657732
SNPshot	rs876657732
SNPdbe	rs876657732
MSV3d	rs876657732
GWAS Ctlg	rs876657732

Max Magnitude

0

ClinVar
Risk	rs876657732(-;-)
Alt	rs876657732(-;-)
Reference	Rs876657732(A;A)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	USH2A
CLNDBN	Usher syndrome, type 2A
Reversed	1
HGVS	NC_000001.10:g.216172247delT
CLNSRC
CLNACC	RCV000217100.1,