rs61755789

Orientation

minus

Stabilized

minus

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

Make rs61755789(A;A)

Make rs61755789(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42721835

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755789
dbSNP (classic)	rs61755789
ClinGen	rs61755789
ebi	rs61755789
HLI	rs61755789
Exac	rs61755789
Gnomad	rs61755789
Varsome	rs61755789
LitVar	rs61755789
Map	rs61755789
PheGenI	rs61755789
Biobank	rs61755789
1000 genomes	rs61755789
hgdp	rs61755789
ensembl	rs61755789
geneview	rs61755789
scholar	rs61755789
google	rs61755789
pharmgkb	rs61755789
gwascentral	rs61755789
openSNP	rs61755789
23andMe	rs61755789
SNPshot	rs61755789
SNPdbe	rs61755789
MSV3d	rs61755789
GWAS Ctlg	rs61755789

Max Magnitude

0

OMIM	179605
Desc
Variant	0009
Related	also

ClinVar
Risk	rs61755789(A;A)
Alt	rs61755789(A;A)
Reference	Rs61755789(G;G)
Significance	Pathogenic
Disease	Patterned dystrophy of retinal pigment epithelium not provided
Variation	info
Gene	PRPH2
CLNDBN	Patterned dystrophy of retinal pigment epithelium not provided
Reversed	1
HGVS	NC_000006.11:g.42689573C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014055.25, RCV000084977.1,