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rs794728242

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728242(A;G)
Make rs794728242(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48444660
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728242
ebirs794728242
HLIrs794728242
Exacrs794728242
Varsomers794728242
Maprs794728242
PheGenIrs794728242
hapmaprs794728242
1000 genomesrs794728242
hgdprs794728242
ensemblrs794728242
gopubmedrs794728242
geneviewrs794728242
scholarrs794728242
googlers794728242
pharmgkbrs794728242
gwascentralrs794728242
openSNPrs794728242
23andMers794728242
23andMe allrs794728242
SNP Nexus

SNPshotrs794728242
SNPdbers794728242
MSV3drs794728242
GWAS Ctlgrs794728242
Max Magnitude0
ClinVar
Risk rs794728242(G;G)
Alt rs794728242(G;G)
Reference rs794728242(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48736857T>C
CLNSRC
CLNACC RCV000181554.2,