rs61755816

Orientation

minus

Stabilized

minus

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

Make rs61755816(A;A)

Make rs61755816(A;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42704461

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755816
dbSNP (classic)	rs61755816
ClinGen	rs61755816
ebi	rs61755816
HLI	rs61755816
Exac	rs61755816
Gnomad	rs61755816
Varsome	rs61755816
LitVar	rs61755816
Map	rs61755816
PheGenI	rs61755816
Biobank	rs61755816
1000 genomes	rs61755816
hgdp	rs61755816
ensembl	rs61755816
geneview	rs61755816
scholar	rs61755816
google	rs61755816
pharmgkb	rs61755816
gwascentral	rs61755816
openSNP	rs61755816
23andMe	rs61755816
SNPshot	rs61755816
SNPdbe	rs61755816
MSV3d	rs61755816
GWAS Ctlg	rs61755816

Max Magnitude

0

OMIM	179605
Desc
Variant	0011
Related	also

ClinVar
Risk	rs61755816(A;A) rs61755816(G;G)
Alt	rs61755816(A;A) rs61755816(G;G)
Reference	Rs61755816(C;C)
Significance	Pathogenic
Disease	not provided Retinitis pigmentosa 7
Variation	info
Gene	PRPH2
CLNDBN	not provided Retinitis pigmentosa 7
Reversed	1
HGVS	NC_000006.11:g.42672199G>C; NC_000006.11:g.42672199G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000085018.1, RCV000014058.18, RCV000085017.1,