rs886043626

Orientation

plus

Stabilized

plus

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

Chromosome

17

Position

74919525

Gene

USH1G

is a	snp
is	mentioned by
dbSNP	rs886043626
dbSNP (classic)	rs886043626
ClinGen	rs886043626
ebi	rs886043626
HLI	rs886043626
Exac	rs886043626
Gnomad	rs886043626
Varsome	rs886043626
LitVar	rs886043626
Map	rs886043626
PheGenI	rs886043626
Biobank	rs886043626
1000 genomes	rs886043626
hgdp	rs886043626
ensembl	rs886043626
geneview	rs886043626
scholar	rs886043626
google	rs886043626
pharmgkb	rs886043626
gwascentral	rs886043626
openSNP	rs886043626
23andMe	rs886043626
SNPshot	rs886043626
SNPdbe	rs886043626
MSV3d	rs886043626
GWAS Ctlg	rs886043626

Max Magnitude

0

ClinVar
Risk	rs886043626(-;-)
Alt	rs886043626(-;-)
Reference	Rs886043626(C;C)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	USH1G
CLNDBN	Usher syndrome, type 1G
Reversed	0
HGVS	NC_000017.10:g.72915620delC
CLNSRC
CLNACC	RCV000333423.1,