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rs794728209

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728209(A;A)
Make rs794728209(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48485373
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728209
ebirs794728209
HLIrs794728209
Exacrs794728209
Varsomers794728209
Maprs794728209
PheGenIrs794728209
hapmaprs794728209
1000 genomesrs794728209
hgdprs794728209
ensemblrs794728209
gopubmedrs794728209
geneviewrs794728209
scholarrs794728209
googlers794728209
pharmgkbrs794728209
gwascentralrs794728209
openSNPrs794728209
23andMers794728209
23andMe allrs794728209
SNP Nexus

SNPshotrs794728209
SNPdbers794728209
MSV3drs794728209
GWAS Ctlgrs794728209
Max Magnitude0
ClinVar
Risk rs794728209(A;A)
Alt rs794728209(A;A)
Reference rs794728209(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48777570C>T
CLNSRC
CLNACC RCV000181494.2,