rs104894037

Orientation

minus

Stabilized

minus

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

Make rs104894037(A;T)

Make rs104894037(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

33096550

Gene

RP9

is a	snp
is	mentioned by
dbSNP	rs104894037
dbSNP (classic)	rs104894037
ClinGen	rs104894037
ebi	rs104894037
HLI	rs104894037
Exac	rs104894037
Gnomad	rs104894037
Varsome	rs104894037
LitVar	rs104894037
Map	rs104894037
PheGenI	rs104894037
Biobank	rs104894037
1000 genomes	rs104894037
hgdp	rs104894037
ensembl	rs104894037
geneview	rs104894037
scholar	rs104894037
google	rs104894037
pharmgkb	rs104894037
gwascentral	rs104894037
openSNP	rs104894037
23andMe	rs104894037
SNPshot	rs104894037
SNPdbe	rs104894037
MSV3d	rs104894037
GWAS Ctlg	rs104894037

Max Magnitude

0

OMIM	607331
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894037(T;T)
Alt	rs104894037(T;T)
Reference	Rs104894037(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 9
Variation	info
Gene	RP9
CLNDBN	Retinitis pigmentosa 9
Reversed	1
HGVS	NC_000007.13:g.33136162T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003498.3,