rs199476183

Orientation

plus

Stabilized

plus

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

Make rs199476183(A;G)

Make rs199476183(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

186208863

Gene

CYP4V2

is a	snp
is	mentioned by
dbSNP	rs199476183
dbSNP (classic)	rs199476183
ClinGen	rs199476183
ebi	rs199476183
HLI	rs199476183
Exac	rs199476183
Gnomad	rs199476183
Varsome	rs199476183
LitVar	rs199476183
Map	rs199476183
PheGenI	rs199476183
Biobank	rs199476183
1000 genomes	rs199476183
hgdp	rs199476183
ensembl	rs199476183
geneview	rs199476183
scholar	rs199476183
google	rs199476183
pharmgkb	rs199476183
gwascentral	rs199476183
openSNP	rs199476183
23andMe	rs199476183
SNPshot	rs199476183
SNPdbe	rs199476183
MSV3d	rs199476183
GWAS Ctlg	rs199476183

Max Magnitude

0

ClinVar
Risk	rs199476183(G;G)
Alt	rs199476183(G;G)
Reference	Rs199476183(A;A)
Significance	Pathogenic
Disease	Bietti crystalline corneoretinal dystrophy
Variation	info
Gene	CYP4V2
CLNDBN	Bietti crystalline corneoretinal dystrophy
Reversed	0
HGVS	NC_000004.11:g.187130017A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002275.6,