rs61755807

Orientation

minus

Stabilized

minus

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

Make rs61755807(-;-)

Make rs61755807(-;CAC)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

42704535

Gene

PRPH2

is a	snp
is	mentioned by
dbSNP	rs61755807
dbSNP (classic)	rs61755807
ClinGen	rs61755807
ebi	rs61755807
HLI	rs61755807
Exac	rs61755807
Gnomad	rs61755807
Varsome	rs61755807
LitVar	rs61755807
Map	rs61755807
PheGenI	rs61755807
Biobank	rs61755807
1000 genomes	rs61755807
hgdp	rs61755807
ensembl	rs61755807
geneview	rs61755807
scholar	rs61755807
google	rs61755807
pharmgkb	rs61755807
gwascentral	rs61755807
openSNP	rs61755807
23andMe	rs61755807
SNPshot	rs61755807
SNPdbe	rs61755807
MSV3d	rs61755807
GWAS Ctlg	rs61755807

Merged from

Rs121918562

Max Magnitude

0

ClinVar
Risk	rs61755807(CCA;CCA) rs61755807(-;-)
Alt	rs61755807(CCA;CCA) rs61755807(-;-)
Reference	Rs61755807(CAC;CAC)
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.42672273_42672275delGTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014049.18, RCV000085009.1,