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rs794728170

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728170(A;A)
Make rs794728170(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48513554
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728170
ebirs794728170
HLIrs794728170
Exacrs794728170
Varsomers794728170
Maprs794728170
PheGenIrs794728170
hapmaprs794728170
1000 genomesrs794728170
hgdprs794728170
ensemblrs794728170
gopubmedrs794728170
geneviewrs794728170
scholarrs794728170
googlers794728170
pharmgkbrs794728170
gwascentralrs794728170
openSNPrs794728170
23andMers794728170
23andMe allrs794728170
SNP Nexus

SNPshotrs794728170
SNPdbers794728170
MSV3drs794728170
GWAS Ctlgrs794728170
Max Magnitude0
ClinVar
Risk rs794728170(A;A)
Alt rs794728170(A;A)
Reference rs794728170(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48805751C>T
CLNSRC
CLNACC RCV000181435.1,