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

rs794728221

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728221(A;A)
Make rs794728221(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48472551
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728221
ebirs794728221
HLIrs794728221
Exacrs794728221
Varsomers794728221
Maprs794728221
PheGenIrs794728221
hapmaprs794728221
1000 genomesrs794728221
hgdprs794728221
ensemblrs794728221
gopubmedrs794728221
geneviewrs794728221
scholarrs794728221
googlers794728221
pharmgkbrs794728221
gwascentralrs794728221
openSNPrs794728221
23andMers794728221
23andMe allrs794728221
SNP Nexus

SNPshotrs794728221
SNPdbers794728221
MSV3drs794728221
GWAS Ctlgrs794728221
Max Magnitude0
ClinVar
Risk rs794728221(A;A)
Alt rs794728221(A;A)
Reference rs794728221(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48764748C>T
CLNSRC
CLNACC RCV000181518.2,