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rs794728189

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728189(A;C)
Make rs794728189(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48496216
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728189
ebirs794728189
HLIrs794728189
Exacrs794728189
Varsomers794728189
Maprs794728189
PheGenIrs794728189
hapmaprs794728189
1000 genomesrs794728189
hgdprs794728189
ensemblrs794728189
gopubmedrs794728189
geneviewrs794728189
scholarrs794728189
googlers794728189
pharmgkbrs794728189
gwascentralrs794728189
openSNPrs794728189
23andMers794728189
23andMe allrs794728189
SNP Nexus

SNPshotrs794728189
SNPdbers794728189
MSV3drs794728189
GWAS Ctlgrs794728189
Max Magnitude0
ClinVar
Risk rs794728189(C;C)
Alt rs794728189(C;C)
Reference rs794728189(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.48788413T>G
CLNSRC
CLNACC RCV000181458.3,