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rs149054177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs149054177(A;G)
Make rs149054177(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position128335562
GeneFBN2
is asnp
is mentioned by
dbSNPrs149054177
ebirs149054177
HLIrs149054177
Exacrs149054177
Varsomers149054177
Maprs149054177
PheGenIrs149054177
hapmaprs149054177
1000 genomesrs149054177
hgdprs149054177
ensemblrs149054177
gopubmedrs149054177
geneviewrs149054177
scholarrs149054177
googlers149054177
pharmgkbrs149054177
gwascentralrs149054177
openSNPrs149054177
23andMers149054177
23andMe allrs149054177
SNP Nexus

SNPshotrs149054177
SNPdbers149054177
MSV3drs149054177
GWAS Ctlgrs149054177
Max Magnitude0
ClinVar
Risk rs149054177(G;G)
Alt rs149054177(G;G)
Reference rs149054177(A;A)
Significance Pathogenic
Disease Macular degeneration not specified
Variation info
Gene FBN2
CLNDBN Macular degeneration, early-onset not specified
Reversed 0
HGVS NC_000005.9:g.127671254A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000148949.3, RCV000200814.2,