rs199476189

Orientation

plus

Stabilized

plus

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

Make rs199476189(G;T)

Make rs199476189(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

186196075

Gene

CYP4V2

is a	snp
is	mentioned by
dbSNP	rs199476189
dbSNP (classic)	rs199476189
ClinGen	rs199476189
ebi	rs199476189
HLI	rs199476189
Exac	rs199476189
Gnomad	rs199476189
Varsome	rs199476189
LitVar	rs199476189
Map	rs199476189
PheGenI	rs199476189
Biobank	rs199476189
1000 genomes	rs199476189
hgdp	rs199476189
ensembl	rs199476189
geneview	rs199476189
scholar	rs199476189
google	rs199476189
pharmgkb	rs199476189
gwascentral	rs199476189
openSNP	rs199476189
23andMe	rs199476189
SNPshot	rs199476189
SNPdbe	rs199476189
MSV3d	rs199476189
GWAS Ctlg	rs199476189

Max Magnitude

0

ClinVar
Risk	rs199476189(T;T)
Alt	rs199476189(T;T)
Reference	Rs199476189(G;G)
Significance	Pathogenic
Disease	Bietti crystalline corneoretinal dystrophy
Variation	info
Gene	CYP4V2
CLNDBN	Bietti crystalline corneoretinal dystrophy
Reversed	0
HGVS	NC_000004.11:g.187117229G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032542.2,