Rs121434301

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434301(C;T)
Make rs121434301(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position91937067
GeneFBLN5, LOC102724531
is asnp
is mentioned by
dbSNPrs121434301
Exacrs121434301
PheGenIrs121434301
nextbiors121434301
hapmaprs121434301
1000 genomesrs121434301
hgdprs121434301
ensemblrs121434301
gopubmedrs121434301
geneviewrs121434301
scholarrs121434301
googlers121434301
pharmgkbrs121434301
gwascentralrs121434301
openSNPrs121434301
23andMers121434301
23andMe allrs121434301
SNP Nexus

SNPshotrs121434301
SNPdbers121434301
MSV3drs121434301
Merged fromRs28939373
OMIM604580
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121434301(T;T)
Alt rs121434301(T;T)
Reference rs121434301(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.92403411G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005813.1,