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rs794728225

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728225(A;A)
Make rs794728225(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48468474
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728225
ebirs794728225
HLIrs794728225
Exacrs794728225
Varsomers794728225
Maprs794728225
PheGenIrs794728225
hapmaprs794728225
1000 genomesrs794728225
hgdprs794728225
ensemblrs794728225
gopubmedrs794728225
geneviewrs794728225
scholarrs794728225
googlers794728225
pharmgkbrs794728225
gwascentralrs794728225
openSNPrs794728225
23andMers794728225
23andMe allrs794728225
SNP Nexus

SNPshotrs794728225
SNPdbers794728225
MSV3drs794728225
GWAS Ctlgrs794728225
Max Magnitude0
ClinVar
Risk rs794728225(A;A)
Alt rs794728225(A;A)
Reference rs794728225(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48760671C>T
CLNSRC
CLNACC RCV000181525.1,