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rs794728237

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728237(A;A)
Make rs794728237(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48446795
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728237
ebirs794728237
HLIrs794728237
Exacrs794728237
Varsomers794728237
Maprs794728237
PheGenIrs794728237
hapmaprs794728237
1000 genomesrs794728237
hgdprs794728237
ensemblrs794728237
gopubmedrs794728237
geneviewrs794728237
scholarrs794728237
googlers794728237
pharmgkbrs794728237
gwascentralrs794728237
openSNPrs794728237
23andMers794728237
23andMe allrs794728237
SNP Nexus

SNPshotrs794728237
SNPdbers794728237
MSV3drs794728237
GWAS Ctlgrs794728237
Max Magnitude0
ClinVar
Risk rs794728237(A;A)
Alt rs794728237(A;A)
Reference rs794728237(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48738992C>T
CLNSRC
CLNACC RCV000181547.1,