rs775098953

Orientation

plus

Stabilized

plus

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

Make rs775098953(A;C)

Make rs775098953(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

150928174

Gene

CLRN1

is a	snp
is	mentioned by
dbSNP	rs775098953
dbSNP (classic)	rs775098953
ClinGen	rs775098953
ebi	rs775098953
HLI	rs775098953
Exac	rs775098953
Gnomad	rs775098953
Varsome	rs775098953
LitVar	rs775098953
Map	rs775098953
PheGenI	rs775098953
Biobank	rs775098953
1000 genomes	rs775098953
hgdp	rs775098953
ensembl	rs775098953
geneview	rs775098953
scholar	rs775098953
google	rs775098953
pharmgkb	rs775098953
gwascentral	rs775098953
openSNP	rs775098953
23andMe	rs775098953
SNPshot	rs775098953
SNPdbe	rs775098953
MSV3d	rs775098953
GWAS Ctlg	rs775098953

Max Magnitude

0

ClinVar
Risk	rs775098953(C;C)
Alt	rs775098953(C;C)
Reference	Rs775098953(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 61
Variation	info
Gene	CLRN1
CLNDBN	Retinitis pigmentosa 61
Reversed	0
HGVS	NC_000003.11:g.150645961A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023537.2,