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rs61734479

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61734479(C;T)
Make rs61734479(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position91936950
GeneFBLN5
is asnp
is mentioned by
dbSNPrs61734479
ebirs61734479
HLIrs61734479
Exacrs61734479
Varsomers61734479
Maprs61734479
PheGenIrs61734479
hapmaprs61734479
1000 genomesrs61734479
hgdprs61734479
ensemblrs61734479
gopubmedrs61734479
geneviewrs61734479
scholarrs61734479
googlers61734479
pharmgkbrs61734479
gwascentralrs61734479
openSNPrs61734479
23andMers61734479
23andMe allrs61734479
SNP Nexus

SNPshotrs61734479
SNPdbers61734479
MSV3drs61734479
GWAS Ctlgrs61734479
Max Magnitude0
ClinVar
Risk rs61734479(T;T)
Alt rs61734479(T;T)
Reference rs61734479(C;C)
Significance Pathogenic
Disease Age-related macular degeneration 3
Variation info
Gene FBLN5
CLNDBN Age-related macular degeneration 3
Reversed 0
HGVS NC_000014.8:g.92403294C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202603.1,