rs199476182

Orientation

plus

Stabilized

plus

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

Make rs199476182(A;A)

Make rs199476182(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

186194613

Gene

CYP4V2

is a	snp
is	mentioned by
dbSNP	rs199476182
dbSNP (classic)	rs199476182
ClinGen	rs199476182
ebi	rs199476182
HLI	rs199476182
Exac	rs199476182
Gnomad	rs199476182
Varsome	rs199476182
LitVar	rs199476182
Map	rs199476182
PheGenI	rs199476182
Biobank	rs199476182
1000 genomes	rs199476182
hgdp	rs199476182
ensembl	rs199476182
geneview	rs199476182
scholar	rs199476182
google	rs199476182
pharmgkb	rs199476182
gwascentral	rs199476182
openSNP	rs199476182
23andMe	rs199476182
SNPshot	rs199476182
SNPdbe	rs199476182
MSV3d	rs199476182
GWAS Ctlg	rs199476182

Max Magnitude

0

ClinVar
Risk	rs199476182(A;A)
Alt	rs199476182(A;A)
Reference	Rs199476182(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.187115767G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032539.2,