rs397517932

Orientation

minus

Stabilized

minus

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

Make rs397517932(-;-)

Make rs397517932(-;GTCAT)

Reference

GRCh38 38.1/141

Chromosome

3

Position

150941710

Gene

CLRN1

is a	snp
is	mentioned by
dbSNP	rs397517932
dbSNP (classic)	rs397517932
ClinGen	rs397517932
ebi	rs397517932
HLI	rs397517932
Exac	rs397517932
Gnomad	rs397517932
Varsome	rs397517932
LitVar	rs397517932
Map	rs397517932
PheGenI	rs397517932
Biobank	rs397517932
1000 genomes	rs397517932
hgdp	rs397517932
ensembl	rs397517932
geneview	rs397517932
scholar	rs397517932
google	rs397517932
pharmgkb	rs397517932
gwascentral	rs397517932
openSNP	rs397517932
23andMe	rs397517932
SNPshot	rs397517932
SNPdbe	rs397517932
MSV3d	rs397517932
GWAS Ctlg	rs397517932

Max Magnitude

0

ClinVar
Risk	rs397517932(-;-)
Alt	rs397517932(-;-)
Reference	Rs397517932(GTCAT;GTCAT)
Significance	Other
Disease	Usher syndrome
Variation	info
Gene	CLRN1
CLNDBN	Usher syndrome, type 3A
Reversed	1
HGVS	NC_000003.11:g.150659497_150659501delATGAC
CLNSRC	Counsyl
CLNACC	RCV000041435.4,