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rs794728215

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728215(A;A)
Make rs794728215(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48474553
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728215
ebirs794728215
HLIrs794728215
Exacrs794728215
Varsomers794728215
Maprs794728215
PheGenIrs794728215
hapmaprs794728215
1000 genomesrs794728215
hgdprs794728215
ensemblrs794728215
gopubmedrs794728215
geneviewrs794728215
scholarrs794728215
googlers794728215
pharmgkbrs794728215
gwascentralrs794728215
openSNPrs794728215
23andMers794728215
23andMe allrs794728215
SNP Nexus

SNPshotrs794728215
SNPdbers794728215
MSV3drs794728215
GWAS Ctlgrs794728215
Max Magnitude0
ClinVar
Risk rs794728215(A;A)
Alt rs794728215(A;A)
Reference rs794728215(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48766750C>T
CLNSRC
CLNACC RCV000181505.1,