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rs794728180

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728180(A;C)
Make rs794728180(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48505071
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728180
dbSNP (old)rs794728180
ClinGenrs794728180
ebirs794728180
HLIrs794728180
Exacrs794728180
Gnomadrs794728180
Varsomers794728180
Maprs794728180
PheGenIrs794728180
Biobankrs794728180
1000 genomesrs794728180
hgdprs794728180
ensemblrs794728180
gopubmedrs794728180
geneviewrs794728180
scholarrs794728180
googlers794728180
pharmgkbrs794728180
gwascentralrs794728180
openSNPrs794728180
23andMers794728180
23andMe allrs794728180
SNP Nexus

SNPshotrs794728180
SNPdbers794728180
MSV3drs794728180
GWAS Ctlgrs794728180
Max Magnitude0
ClinVar
Risk rs794728180(C;C)
Alt rs794728180(C;C)
Reference Rs794728180(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.48797268T>G
CLNSRC
CLNACC RCV000181448.2,