rs267607077

Orientation

minus

Stabilized

minus

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

Make rs267607077(C;T)

Make rs267607077(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

96287968

Gene

SNRNP200

is a	snp
is	mentioned by
dbSNP	rs267607077
dbSNP (classic)	rs267607077
ClinGen	rs267607077
ebi	rs267607077
HLI	rs267607077
Exac	rs267607077
Gnomad	rs267607077
Varsome	rs267607077
LitVar	rs267607077
Map	rs267607077
PheGenI	rs267607077
Biobank	rs267607077
1000 genomes	rs267607077
hgdp	rs267607077
ensembl	rs267607077
geneview	rs267607077
scholar	rs267607077
google	rs267607077
pharmgkb	rs267607077
gwascentral	rs267607077
openSNP	rs267607077
23andMe	rs267607077
SNPshot	rs267607077
SNPdbe	rs267607077
MSV3d	rs267607077
GWAS Ctlg	rs267607077

Max Magnitude

0

ClinVar
Risk	rs267607077(T;T)
Alt	rs267607077(T;T)
Reference	Rs267607077(C;C)
Significance	Pathogenic
Disease	Retinitis pigmentosa 33
Variation	info
Gene	SNRNP200
CLNDBN	Retinitis pigmentosa 33
Reversed	1
HGVS	NC_000002.11:g.96953706G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008390.3,