rs876657624

Orientation

minus

Stabilized

minus

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

Make rs876657624(A;A)

Make rs876657624(A;C)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

17544301

Gene

USH1C

is a	snp
is	mentioned by
dbSNP	rs876657624
dbSNP (classic)	rs876657624
ClinGen	rs876657624
ebi	rs876657624
HLI	rs876657624
Exac	rs876657624
Gnomad	rs876657624
Varsome	rs876657624
LitVar	rs876657624
Map	rs876657624
PheGenI	rs876657624
Biobank	rs876657624
1000 genomes	rs876657624
hgdp	rs876657624
ensembl	rs876657624
geneview	rs876657624
scholar	rs876657624
google	rs876657624
pharmgkb	rs876657624
gwascentral	rs876657624
openSNP	rs876657624
23andMe	rs876657624
SNPshot	rs876657624
SNPdbe	rs876657624
MSV3d	rs876657624
GWAS Ctlg	rs876657624

Max Magnitude

0

ClinVar
Risk	rs876657624(A;A) rs876657624(G;G) rs876657624(T;T)
Alt	rs876657624(A;A) rs876657624(G;G) rs876657624(T;T)
Reference	Rs876657624(C;C)
Significance	Pathogenic
Disease	Usher syndrome not specified
Variation	info
Gene	USH1C
CLNDBN	Usher syndrome, type 1C not specified
Reversed	1
HGVS	NC_000011.9:g.17565848G>A; NC_000011.9:g.17565848G>T
CLNSRC
CLNACC	RCV000240666.1, RCV000222607.1,