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rs777526851

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777526851(A;A)
Make rs777526851(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48498999
GeneFBN1
is asnp
is mentioned by
dbSNPrs777526851
ebirs777526851
HLIrs777526851
Exacrs777526851
Varsomers777526851
Maprs777526851
PheGenIrs777526851
hapmaprs777526851
1000 genomesrs777526851
hgdprs777526851
ensemblrs777526851
gopubmedrs777526851
geneviewrs777526851
scholarrs777526851
googlers777526851
pharmgkbrs777526851
gwascentralrs777526851
openSNPrs777526851
23andMers777526851
23andMe allrs777526851
SNP Nexus

SNPshotrs777526851
SNPdbers777526851
MSV3drs777526851
GWAS Ctlgrs777526851
Max Magnitude0
ClinVar
Risk rs777526851(A;A)
Alt rs777526851(A;A)
Reference rs777526851(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48791196G>A
CLNSRC
CLNACC RCV000181454.1,