rs730880268

Orientation

minus

Stabilized

minus

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

Make rs730880268(-;-)

Make rs730880268(-;CA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

74920649

Gene

USH1G

is a	snp
is	mentioned by
dbSNP	rs730880268
dbSNP (classic)	rs730880268
ClinGen	rs730880268
ebi	rs730880268
HLI	rs730880268
Exac	rs730880268
Gnomad	rs730880268
Varsome	rs730880268
LitVar	rs730880268
Map	rs730880268
PheGenI	rs730880268
Biobank	rs730880268
1000 genomes	rs730880268
hgdp	rs730880268
ensembl	rs730880268
geneview	rs730880268
scholar	rs730880268
google	rs730880268
pharmgkb	rs730880268
gwascentral	rs730880268
openSNP	rs730880268
23andMe	rs730880268
SNPshot	rs730880268
SNPdbe	rs730880268
MSV3d	rs730880268
GWAS Ctlg	rs730880268

Max Magnitude

0

ClinVar
Risk	rs730880268(-;-)
Alt	rs730880268(-;-)
Reference	Rs730880268(CA;CA)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	USH1G
CLNDBN	Usher syndrome, type 1G
Reversed	1
HGVS	NC_000017.10:g.72916744_72916745delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003049.3,