rs374963432

Orientation

plus

Stabilized

plus

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

Make rs374963432(G;T)

Make rs374963432(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

150941647

Gene

CLRN1

is a	snp
is	mentioned by
dbSNP	rs374963432
dbSNP (classic)	rs374963432
ClinGen	rs374963432
ebi	rs374963432
HLI	rs374963432
Exac	rs374963432
Gnomad	rs374963432
Varsome	rs374963432
LitVar	rs374963432
Map	rs374963432
PheGenI	rs374963432
Biobank	rs374963432
1000 genomes	rs374963432
hgdp	rs374963432
ensembl	rs374963432
geneview	rs374963432
scholar	rs374963432
google	rs374963432
pharmgkb	rs374963432
gwascentral	rs374963432
openSNP	rs374963432
23andMe	rs374963432
SNPshot	rs374963432
SNPdbe	rs374963432
MSV3d	rs374963432
GWAS Ctlg	rs374963432

Max Magnitude

0

ClinVar
Risk	rs374963432(T;T)
Alt	rs374963432(T;T)
Reference	Rs374963432(G;G)
Significance	Other
Disease	Usher syndrome
Variation	info
Gene	CLRN1
CLNDBN	Usher syndrome, type 3A
Reversed	0
HGVS	NC_000003.11:g.150659434G>T
CLNSRC	ClinVar
CLNACC	RCV000041436.4,