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rs770484928

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770484928(A;A)
Make rs770484928(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48411201
GeneFBN1
is asnp
is mentioned by
dbSNPrs770484928
ebirs770484928
HLIrs770484928
Exacrs770484928
Varsomers770484928
Maprs770484928
PheGenIrs770484928
hapmaprs770484928
1000 genomesrs770484928
hgdprs770484928
ensemblrs770484928
gopubmedrs770484928
geneviewrs770484928
scholarrs770484928
googlers770484928
pharmgkbrs770484928
gwascentralrs770484928
openSNPrs770484928
23andMers770484928
23andMe allrs770484928
SNP Nexus

SNPshotrs770484928
SNPdbers770484928
MSV3drs770484928
GWAS Ctlgrs770484928
Max Magnitude0
ClinVar
Risk rs770484928(A;A)
Alt rs770484928(A;A)
Reference rs770484928(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48703398C>T
CLNSRC
CLNACC RCV000181631.2,