rs104894082

Orientation

plus

Stabilized

plus

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

Make rs104894082(C;T)

Make rs104894082(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

54625911

Gene

RP1

is a	snp
is	mentioned by
dbSNP	rs104894082
dbSNP (classic)	rs104894082
ClinGen	rs104894082
ebi	rs104894082
HLI	rs104894082
Exac	rs104894082
Gnomad	rs104894082
Varsome	rs104894082
LitVar	rs104894082
Map	rs104894082
PheGenI	rs104894082
Biobank	rs104894082
1000 genomes	rs104894082
hgdp	rs104894082
ensembl	rs104894082
geneview	rs104894082
scholar	rs104894082
google	rs104894082
pharmgkb	rs104894082
gwascentral	rs104894082
openSNP	rs104894082
23andMe	rs104894082
SNPshot	rs104894082
SNPdbe	rs104894082
MSV3d	rs104894082
GWAS Ctlg	rs104894082

Max Magnitude

0

OMIM	603937
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894082(T;T)
Alt	rs104894082(T;T)
Reference	Rs104894082(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 1 not provided
Variation	info
Gene	RP1
CLNDBN	Retinitis pigmentosa 1 not provided
Reversed	0
HGVS	NC_000008.10:g.55538471C>T
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000006329.5, RCV000255140.1,