rs1057516687

Orientation

minus

Stabilized

minus

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

Make rs1057516687(-;T)

Make rs1057516687(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

150941579

Gene

CLRN1

is a	snp
is	mentioned by
dbSNP	rs1057516687
dbSNP (classic)	rs1057516687
ClinGen	rs1057516687
ebi	rs1057516687
HLI	rs1057516687
Exac	rs1057516687
Gnomad	rs1057516687
Varsome	rs1057516687
LitVar	rs1057516687
Map	rs1057516687
PheGenI	rs1057516687
Biobank	rs1057516687
1000 genomes	rs1057516687
hgdp	rs1057516687
ensembl	rs1057516687
geneview	rs1057516687
scholar	rs1057516687
google	rs1057516687
pharmgkb	rs1057516687
gwascentral	rs1057516687
openSNP	rs1057516687
23andMe	rs1057516687
SNPshot	rs1057516687
SNPdbe	rs1057516687
MSV3d	rs1057516687
GWAS Ctlg	rs1057516687

Max Magnitude

0

ClinVar
Risk	rs1057516687(T;T)
Alt	rs1057516687(T;T)
Reference	Rs1057516687(-;-)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	CLRN1
CLNDBN	Usher syndrome, type 3A
Reversed	1
HGVS	NC_000003.11:g.150659367dupA
CLNSRC
CLNACC	RCV000412361.1,