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rs149684063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs149684063(A;G)
Make rs149684063(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position186196042
GeneCYP4V2
is asnp
is mentioned by
dbSNPrs149684063
ebirs149684063
HLIrs149684063
Exacrs149684063
Varsomers149684063
Maprs149684063
PheGenIrs149684063
hapmaprs149684063
1000 genomesrs149684063
hgdprs149684063
ensemblrs149684063
gopubmedrs149684063
geneviewrs149684063
scholarrs149684063
googlers149684063
pharmgkbrs149684063
gwascentralrs149684063
openSNPrs149684063
23andMers149684063
23andMe allrs149684063
SNP Nexus

SNPshotrs149684063
SNPdbers149684063
MSV3drs149684063
GWAS Ctlgrs149684063
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs149684063(G;G)
Alt rs149684063(G;G)
Reference rs149684063(A;A)
Significance Pathogenic
Disease Bietti crystalline corneoretinal dystrophy not provided
Variation info
Gene CYP4V2
CLNDBN Bietti crystalline corneoretinal dystrophy not provided
Reversed 0
HGVS NC_000004.11:g.187117196A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000032541.2, RCV000132718.1,