rs199476196

Orientation

plus

Stabilized

plus

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

Make rs199476196(C;T)

Make rs199476196(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

186201329

Gene

CYP4V2

is a	snp
is	mentioned by
dbSNP	rs199476196
dbSNP (classic)	rs199476196
ClinGen	rs199476196
ebi	rs199476196
HLI	rs199476196
Exac	rs199476196
Gnomad	rs199476196
Varsome	rs199476196
LitVar	rs199476196
Map	rs199476196
PheGenI	rs199476196
Biobank	rs199476196
1000 genomes	rs199476196
hgdp	rs199476196
ensembl	rs199476196
geneview	rs199476196
scholar	rs199476196
google	rs199476196
pharmgkb	rs199476196
gwascentral	rs199476196
openSNP	rs199476196
23andMe	rs199476196
SNPshot	rs199476196
SNPdbe	rs199476196
MSV3d	rs199476196
GWAS Ctlg	rs199476196

Max Magnitude

0

ClinVar
Risk	rs199476196(T;T)
Alt	rs199476196(T;T)
Reference	Rs199476196(C;C)
Significance	Pathogenic
Disease	Bietti crystalline corneoretinal dystrophy
Variation	info
Gene	CYP4V2
CLNDBN	Bietti crystalline corneoretinal dystrophy
Reversed	0
HGVS	NC_000004.11:g.187122483C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000032551.2,