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rs199476182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199476182(A;A)
Make rs199476182(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position186194613
GeneCYP4V2
is asnp
is mentioned by
dbSNPrs199476182
ebirs199476182
HLIrs199476182
Exacrs199476182
Varsomers199476182
Maprs199476182
PheGenIrs199476182
hapmaprs199476182
1000 genomesrs199476182
hgdprs199476182
ensemblrs199476182
gopubmedrs199476182
geneviewrs199476182
scholarrs199476182
googlers199476182
pharmgkbrs199476182
gwascentralrs199476182
openSNPrs199476182
23andMers199476182
23andMe allrs199476182
SNP Nexus

SNPshotrs199476182
SNPdbers199476182
MSV3drs199476182
GWAS Ctlgrs199476182
Max Magnitude0
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,