rs373208120

Orientation

plus

Stabilized

plus

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

Make rs373208120(A;A)

Make rs373208120(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

150928016

Gene

CLRN1

is a	snp
is	mentioned by
dbSNP	rs373208120
dbSNP (classic)	rs373208120
ClinGen	rs373208120
ebi	rs373208120
HLI	rs373208120
Exac	rs373208120
Gnomad	rs373208120
Varsome	rs373208120
LitVar	rs373208120
Map	rs373208120
PheGenI	rs373208120
Biobank	rs373208120
1000 genomes	rs373208120
hgdp	rs373208120
ensembl	rs373208120
geneview	rs373208120
scholar	rs373208120
google	rs373208120
pharmgkb	rs373208120
gwascentral	rs373208120
openSNP	rs373208120
23andMe	rs373208120
SNPshot	rs373208120
SNPdbe	rs373208120
MSV3d	rs373208120
GWAS Ctlg	rs373208120

Max Magnitude

0

ClinVar
Risk	rs373208120(A;A)
Alt	rs373208120(A;A)
Reference	Rs373208120(G;G)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	CLRN1
CLNDBN	Usher syndrome, type 3A
Reversed	0
HGVS	NC_000003.11:g.150645803G>A
CLNSRC
CLNACC	RCV000408993.1,