rs61755794

Orientation

minus

Stabilized

minus

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

Make rs61755794(A;T)

Make rs61755794(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42721817

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755794
dbSNP (classic)	rs61755794
ClinGen	rs61755794
ebi	rs61755794
HLI	rs61755794
Exac	rs61755794
Gnomad	rs61755794
Varsome	rs61755794
LitVar	rs61755794
Map	rs61755794
PheGenI	rs61755794
Biobank	rs61755794
1000 genomes	rs61755794
hgdp	rs61755794
ensembl	rs61755794
geneview	rs61755794
scholar	rs61755794
google	rs61755794
pharmgkb	rs61755794
gwascentral	rs61755794
openSNP	rs61755794
23andMe	rs61755794
SNPshot	rs61755794
SNPdbe	rs61755794
MSV3d	rs61755794
GWAS Ctlg	rs61755794

Max Magnitude

0

OMIM	179605
Desc
Variant	0020
Related	also

ClinVar
Risk	rs61755794(T;T)
Alt	rs61755794(T;T)
Reference	Rs61755794(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 7 not provided
Variation	info
Gene	PRPH2
CLNDBN	Retinitis pigmentosa 7 not provided
Reversed	1
HGVS	NC_000006.11:g.42689555T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014069.18, RCV000084983.1,