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

rs794728208

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728208(A;A)
Make rs794728208(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48485374
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728208
ebirs794728208
HLIrs794728208
Exacrs794728208
Varsomers794728208
Maprs794728208
PheGenIrs794728208
hapmaprs794728208
1000 genomesrs794728208
hgdprs794728208
ensemblrs794728208
gopubmedrs794728208
geneviewrs794728208
scholarrs794728208
googlers794728208
pharmgkbrs794728208
gwascentralrs794728208
openSNPrs794728208
23andMers794728208
23andMe allrs794728208
SNP Nexus

SNPshotrs794728208
SNPdbers794728208
MSV3drs794728208
GWAS Ctlgrs794728208
Max Magnitude0
ClinVar
Risk rs794728208(A;A)
Alt rs794728208(A;A)
Reference rs794728208(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48777571C>T
CLNSRC
CLNACC RCV000181493.2,