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rs794728185

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728185(A;A)
Make rs794728185(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48499005
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728185
ClinGenrs794728185
ebirs794728185
HLIrs794728185
Exacrs794728185
Varsomers794728185
Maprs794728185
PheGenIrs794728185
hapmaprs794728185
1000 genomesrs794728185
hgdprs794728185
ensemblrs794728185
gopubmedrs794728185
geneviewrs794728185
scholarrs794728185
googlers794728185
pharmgkbrs794728185
gwascentralrs794728185
openSNPrs794728185
23andMers794728185
23andMe allrs794728185
SNP Nexus

SNPshotrs794728185
SNPdbers794728185
MSV3drs794728185
GWAS Ctlgrs794728185
Max Magnitude0
ClinVar
Risk rs794728185(A;A)
Alt rs794728185(A;A)
Reference Rs794728185(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48791202C>T
CLNSRC
CLNACC RCV000181453.1,