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rs387906795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906795(G;T)
Make rs387906795(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position20086175
GenePLA2G5
is asnp
is mentioned by
dbSNPrs387906795
ebirs387906795
HLIrs387906795
Exacrs387906795
Varsomers387906795
Maprs387906795
PheGenIrs387906795
hapmaprs387906795
1000 genomesrs387906795
hgdprs387906795
ensemblrs387906795
gopubmedrs387906795
geneviewrs387906795
scholarrs387906795
googlers387906795
pharmgkbrs387906795
gwascentralrs387906795
openSNPrs387906795
23andMers387906795
23andMe allrs387906795
SNP Nexus

SNPshotrs387906795
SNPdbers387906795
MSV3drs387906795
GWAS Ctlgrs387906795
Max Magnitude0
ClinVar
Risk rs387906795(A,T;A,T)
Alt rs387906795(A,T;A,T)
Reference rs387906795(G;G)
Significance Other
Disease Fleck retina
Variation info
Gene PLA2G5
CLNDBN Fleck retina, familial benign
Reversed 0
HGVS NC_000001.10:g.20412668G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023076.3,