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rs794728193

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728193(A;A)
Make rs794728193(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48495173
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728193
ebirs794728193
HLIrs794728193
Exacrs794728193
Varsomers794728193
Maprs794728193
PheGenIrs794728193
hapmaprs794728193
1000 genomesrs794728193
hgdprs794728193
ensemblrs794728193
gopubmedrs794728193
geneviewrs794728193
scholarrs794728193
googlers794728193
pharmgkbrs794728193
gwascentralrs794728193
openSNPrs794728193
23andMers794728193
23andMe allrs794728193
SNP Nexus

SNPshotrs794728193
SNPdbers794728193
MSV3drs794728193
GWAS Ctlgrs794728193
Max Magnitude0
ClinVar
Risk rs794728193(A;A)
Alt rs794728193(A;A)
Reference rs794728193(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48787370C>T
CLNSRC
CLNACC RCV000181463.1,