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rs794728227

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728227(A;A)
Make rs794728227(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48468099
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728227
ebirs794728227
HLIrs794728227
Exacrs794728227
Varsomers794728227
Maprs794728227
PheGenIrs794728227
hapmaprs794728227
1000 genomesrs794728227
hgdprs794728227
ensemblrs794728227
gopubmedrs794728227
geneviewrs794728227
scholarrs794728227
googlers794728227
pharmgkbrs794728227
gwascentralrs794728227
openSNPrs794728227
23andMers794728227
23andMe allrs794728227
SNP Nexus

SNPshotrs794728227
SNPdbers794728227
MSV3drs794728227
GWAS Ctlgrs794728227
Max Magnitude0
ClinVar
Risk rs794728227(A;A)
Alt rs794728227(A;A)
Reference rs794728227(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48760296G>T
CLNSRC
CLNACC RCV000181527.1,