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rs794728172

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728172(G;T)
Make rs794728172(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48510094
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728172
ebirs794728172
HLIrs794728172
Exacrs794728172
Varsomers794728172
Maprs794728172
PheGenIrs794728172
hapmaprs794728172
1000 genomesrs794728172
hgdprs794728172
ensemblrs794728172
gopubmedrs794728172
geneviewrs794728172
scholarrs794728172
googlers794728172
pharmgkbrs794728172
gwascentralrs794728172
openSNPrs794728172
23andMers794728172
23andMe allrs794728172
SNP Nexus

SNPshotrs794728172
SNPdbers794728172
MSV3drs794728172
GWAS Ctlgrs794728172
Max Magnitude0
ClinVar
Risk rs794728172(T;T)
Alt rs794728172(T;T)
Reference rs794728172(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48802291C>A
CLNSRC
CLNACC RCV000181437.1,