rs61755771

Orientation

minus

Stabilized

minus

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

Make rs61755771(C;T)

Make rs61755771(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42722199

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755771
dbSNP (classic)	rs61755771
ClinGen	rs61755771
ebi	rs61755771
HLI	rs61755771
Exac	rs61755771
Gnomad	rs61755771
Varsome	rs61755771
LitVar	rs61755771
Map	rs61755771
PheGenI	rs61755771
Biobank	rs61755771
1000 genomes	rs61755771
hgdp	rs61755771
ensembl	rs61755771
geneview	rs61755771
scholar	rs61755771
google	rs61755771
pharmgkb	rs61755771
gwascentral	rs61755771
openSNP	rs61755771
23andMe	rs61755771
SNPshot	rs61755771
SNPdbe	rs61755771
MSV3d	rs61755771
GWAS Ctlg	rs61755771

Max Magnitude

0

OMIM	179605
Desc
Variant	0018
Related	also

ClinVar
Risk	rs61755771(T;T)
Alt	rs61755771(T;T)
Reference	Rs61755771(C;C)
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.42689937G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014067.25, RCV000084955.1,