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

rs864309526

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309526(C;T)
Make rs864309526(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position91877555
GeneFBLN5
is asnp
is mentioned by
dbSNPrs864309526
ebirs864309526
HLIrs864309526
Exacrs864309526
Varsomers864309526
Maprs864309526
PheGenIrs864309526
hapmaprs864309526
1000 genomesrs864309526
hgdprs864309526
ensemblrs864309526
gopubmedrs864309526
geneviewrs864309526
scholarrs864309526
googlers864309526
pharmgkbrs864309526
gwascentralrs864309526
openSNPrs864309526
23andMers864309526
23andMe allrs864309526
SNP Nexus

SNPshotrs864309526
SNPdbers864309526
MSV3drs864309526
GWAS Ctlgrs864309526
Max Magnitude0
ClinVar
Risk rs864309526(T;T)
Alt rs864309526(T;T)
Reference rs864309526(C;C)
Significance Pathogenic
Disease Age-related macular degeneration 3
Variation info
Gene FBLN5
CLNDBN Age-related macular degeneration 3
Reversed 1
HGVS NC_000014.8:g.92343899G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000202609.1,