rs587776546

Orientation

minus

Stabilized

minus

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

Make rs587776546(-;C)

Make rs587776546(C;C)

Reference

GRCh38 38.1/142

Chromosome

17

Position

74920441

Gene

USH1G

is a	snp
is	mentioned by
dbSNP	rs587776546
dbSNP (classic)	rs587776546
ClinGen	rs587776546
ebi	rs587776546
HLI	rs587776546
Exac	rs587776546
Gnomad	rs587776546
Varsome	rs587776546
LitVar	rs587776546
Map	rs587776546
PheGenI	rs587776546
Biobank	rs587776546
1000 genomes	rs587776546
hgdp	rs587776546
ensembl	rs587776546
geneview	rs587776546
scholar	rs587776546
google	rs587776546
pharmgkb	rs587776546
gwascentral	rs587776546
openSNP	rs587776546
23andMe	rs587776546
SNPshot	rs587776546
SNPdbe	rs587776546
MSV3d	rs587776546
GWAS Ctlg	rs587776546

Max Magnitude

0

ClinVar
Risk	rs587776546(G;G)
Alt	rs587776546(G;G)
Reference	Rs587776546(-;-)
Significance	Pathogenic
Disease	Usher syndrome Usher syndrome
Variation	info
Gene	USH1G
CLNDBN	Usher syndrome, type 1G Usher syndrome, type 1
Reversed	1
HGVS	NC_000017.10:g.72916537dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003051.4, RCV000222936.1,