Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906796(A;A)
Make rs387906796(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position20086187
GenePLA2G5
is asnp
is mentioned by
dbSNPrs387906796
ebirs387906796
HLIrs387906796
Exacrs387906796
Varsomers387906796
Maprs387906796
PheGenIrs387906796
hapmaprs387906796
1000 genomesrs387906796
hgdprs387906796
ensemblrs387906796
gopubmedrs387906796
geneviewrs387906796
scholarrs387906796
googlers387906796
pharmgkbrs387906796
gwascentralrs387906796
openSNPrs387906796
23andMers387906796
23andMe allrs387906796
SNP Nexus

SNPshotrs387906796
SNPdbers387906796
MSV3drs387906796
GWAS Ctlgrs387906796
Max Magnitude0
ClinVar
Risk rs387906796(A;A)
Alt rs387906796(A;A)
Reference rs387906796(G;G)
Significance Other
Disease Fleck retina
Variation info
Gene PLA2G5
CLNDBN Fleck retina, familial benign
Reversed 0
HGVS NC_000001.10:g.20412680G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023078.4,