Rs121434302

From SNPedia
Jump to: navigation, search

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434302(A;A)
Make rs121434302(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position91877585
GeneFBLN5
is asnp
is mentioned by
dbSNPrs121434302
Exacrs121434302
PheGenIrs121434302
nextbiors121434302
hapmaprs121434302
1000 genomesrs121434302
hgdprs121434302
ensemblrs121434302
gopubmedrs121434302
geneviewrs121434302
scholarrs121434302
googlers121434302
pharmgkbrs121434302
gwascentralrs121434302
openSNPrs121434302
23andMers121434302
23andMe allrs121434302
SNP Nexus

SNPshotrs121434302
SNPdbers121434302
MSV3drs121434302
Merged fromRs28939074
OMIM604580
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121434302(A;A)
Alt rs121434302(A;A)
Reference rs121434302(G;G)
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.92343929C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005816.1,