Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728256

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728256(A;A)
Make rs794728256(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48430790
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728256
ebirs794728256
HLIrs794728256
Exacrs794728256
Varsomers794728256
Maprs794728256
PheGenIrs794728256
hapmaprs794728256
1000 genomesrs794728256
hgdprs794728256
ensemblrs794728256
gopubmedrs794728256
geneviewrs794728256
scholarrs794728256
googlers794728256
pharmgkbrs794728256
gwascentralrs794728256
openSNPrs794728256
23andMers794728256
23andMe allrs794728256
SNP Nexus

SNPshotrs794728256
SNPdbers794728256
MSV3drs794728256
GWAS Ctlgrs794728256
Max Magnitude0
ClinVar
Risk rs794728256(A;A)
Alt rs794728256(A;A)
Reference rs794728256(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48722987C>T
CLNSRC
CLNACC RCV000181579.1,