rs199476191

Orientation

plus

Stabilized

plus

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

Make rs199476191(C;C)

Make rs199476191(C;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

186197583

Gene

CYP4V2

is a	snp
is	mentioned by
dbSNP	rs199476191
dbSNP (classic)	rs199476191
ClinGen	rs199476191
ebi	rs199476191
HLI	rs199476191
Exac	rs199476191
Gnomad	rs199476191
Varsome	rs199476191
LitVar	rs199476191
Map	rs199476191
PheGenI	rs199476191
Biobank	rs199476191
1000 genomes	rs199476191
hgdp	rs199476191
ensembl	rs199476191
geneview	rs199476191
scholar	rs199476191
google	rs199476191
pharmgkb	rs199476191
gwascentral	rs199476191
openSNP	rs199476191
23andMe	rs199476191
SNPshot	rs199476191
SNPdbe	rs199476191
MSV3d	rs199476191
GWAS Ctlg	rs199476191

Max Magnitude

0

ClinVar
Risk	rs199476191(C;C)
Alt	rs199476191(C;C)
Reference	Rs199476191(T;T)
Significance	Pathogenic
Disease	Bietti crystalline corneoretinal dystrophy
Variation	info
Gene	CYP4V2
CLNDBN	Bietti crystalline corneoretinal dystrophy
Reversed	0
HGVS	NC_000004.11:g.187118737T>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032545.2,