rs104894671

Orientation

plus

Stabilized

plus

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

Make rs104894671(A;C)

Make rs104894671(C;C)

Reference

GRCh38 38.1/141

Chromosome

19

Position

47836381

Gene

CRX

is a	snp
is	mentioned by
dbSNP	rs104894671
dbSNP (classic)	rs104894671
ClinGen	rs104894671
ebi	rs104894671
HLI	rs104894671
Exac	rs104894671
Gnomad	rs104894671
Varsome	rs104894671
LitVar	rs104894671
Map	rs104894671
PheGenI	rs104894671
Biobank	rs104894671
1000 genomes	rs104894671
hgdp	rs104894671
ensembl	rs104894671
geneview	rs104894671
scholar	rs104894671
google	rs104894671
pharmgkb	rs104894671
gwascentral	rs104894671
openSNP	rs104894671
23andMe	rs104894671
SNPshot	rs104894671
SNPdbe	rs104894671
MSV3d	rs104894671
GWAS Ctlg	rs104894671

Merged from

Rs28939682

Max Magnitude

0

OMIM	602225
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894671(C;C)
Alt	rs104894671(C;C)
Reference	Rs104894671(A;A)
Significance	Pathogenic
Disease	Cone-rod dystrophy 2 not provided
Variation	info
Gene	CRX
CLNDBN	Cone-rod dystrophy 2 not provided
Reversed	0
HGVS	NC_000019.9:g.48339638A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007841.3, RCV000085995.1,