rs61755793

Orientation

minus

Stabilized

minus

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

Make rs61755793(A;A)

Make rs61755793(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42721820

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755793
dbSNP (classic)	rs61755793
ClinGen	rs61755793
ebi	rs61755793
HLI	rs61755793
Exac	rs61755793
Gnomad	rs61755793
Varsome	rs61755793
LitVar	rs61755793
Map	rs61755793
PheGenI	rs61755793
Biobank	rs61755793
1000 genomes	rs61755793
hgdp	rs61755793
ensembl	rs61755793
geneview	rs61755793
scholar	rs61755793
google	rs61755793
pharmgkb	rs61755793
gwascentral	rs61755793
openSNP	rs61755793
23andMe	rs61755793
SNPshot	rs61755793
SNPdbe	rs61755793
MSV3d	rs61755793
GWAS Ctlg	rs61755793

Max Magnitude

0

OMIM	179605
Desc
Variant	0006
Related	also

ClinVar
Risk	rs61755793(A;A)
Alt	rs61755793(A;A)
Reference	Rs61755793(G;G)
Significance	Pathogenic
Disease	Choroidal dystrophy not provided
Variation	info
Gene	PRPH2
CLNDBN	Choroidal dystrophy, central areolar 2 not provided
Reversed	1
HGVS	NC_000006.11:g.42689558C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014053.19, RCV000084982.1,