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rs794728213

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728213(A;A)
Make rs794728213(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48644605
GeneFBN1, LOC105370809
is asnp
is mentioned by
dbSNPrs794728213
ebirs794728213
HLIrs794728213
Exacrs794728213
Varsomers794728213
Maprs794728213
PheGenIrs794728213
hapmaprs794728213
1000 genomesrs794728213
hgdprs794728213
ensemblrs794728213
gopubmedrs794728213
geneviewrs794728213
scholarrs794728213
googlers794728213
pharmgkbrs794728213
gwascentralrs794728213
openSNPrs794728213
23andMers794728213
23andMe allrs794728213
SNP Nexus

SNPshotrs794728213
SNPdbers794728213
MSV3drs794728213
GWAS Ctlgrs794728213
Max Magnitude0
ClinVar
Risk rs794728213(A;A)
Alt rs794728213(A;A)
Reference rs794728213(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48936802C>T
CLNSRC
CLNACC RCV000181502.1,