rs121918562

Merged into

rs61755807

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CAC;CAC)	0	common in clinvar
(CCA;CCA)	0	common/normal

Make rs121918562(-;-)

Make rs121918562(-;CCA)

Reference

GRCh38 38.1/141

Chromosome

6

Position

42704536

Gene	LOC101929618, PRPH2

is a	snp
is	mentioned by
dbSNP	rs121918562
dbSNP (classic)	rs121918562
ClinGen	rs121918562
ebi	rs121918562
HLI	rs121918562
Exac	rs121918562
Gnomad	rs121918562
Varsome	rs121918562
LitVar	rs121918562
Map	rs121918562
PheGenI	rs121918562
Biobank	rs121918562
1000 genomes	rs121918562
hgdp	rs121918562
ensembl	rs121918562
geneview	rs121918562
scholar	rs121918562
google	rs121918562
pharmgkb	rs121918562
gwascentral	rs121918562
openSNP	rs121918562
23andMe	rs121918562
SNPshot	rs121918562
SNPdbe	rs121918562
MSV3d	rs121918562
GWAS Ctlg	rs121918562

Status

Merged into rs61755807

Max Magnitude

0

OMIM	179605
Desc
Variant	0002
Related	also

ClinVar
Risk
Alt
Reference	Rs121918562(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,