rs527236115

Orientation

minus

Stabilized

minus

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

Make rs527236115(A;A)

Make rs527236115(A;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

96293481

Gene

SNRNP200

is a	snp
is	mentioned by
dbSNP	rs527236115
dbSNP (classic)	rs527236115
ClinGen	rs527236115
ebi	rs527236115
HLI	rs527236115
Exac	rs527236115
Gnomad	rs527236115
Varsome	rs527236115
LitVar	rs527236115
Map	rs527236115
PheGenI	rs527236115
Biobank	rs527236115
1000 genomes	rs527236115
hgdp	rs527236115
ensembl	rs527236115
geneview	rs527236115
scholar	rs527236115
google	rs527236115
pharmgkb	rs527236115
gwascentral	rs527236115
openSNP	rs527236115
23andMe	rs527236115
SNPshot	rs527236115
SNPdbe	rs527236115
MSV3d	rs527236115
GWAS Ctlg	rs527236115

Max Magnitude

0

ClinVar
Risk	rs527236115(A;A)
Alt	rs527236115(A;A)
Reference	Rs527236115(G;G)
Significance	Probable-Pathogenic
Disease	Retinitis pigmentosa Retinal dystrophy
Variation	info
Gene	SNRNP200
CLNDBN	Retinitis pigmentosa Retinal dystrophy
Reversed	1
HGVS	NC_000002.11:g.96959219C>T
CLNSRC	ClinVar
CLNACC	RCV000132668.1, RCV000225495.1,