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rs794728250

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728250(G;T)
Make rs794728250(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437008
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728250
ebirs794728250
HLIrs794728250
Exacrs794728250
Varsomers794728250
Maprs794728250
PheGenIrs794728250
hapmaprs794728250
1000 genomesrs794728250
hgdprs794728250
ensemblrs794728250
gopubmedrs794728250
geneviewrs794728250
scholarrs794728250
googlers794728250
pharmgkbrs794728250
gwascentralrs794728250
openSNPrs794728250
23andMers794728250
23andMe allrs794728250
SNP Nexus

SNPshotrs794728250
SNPdbers794728250
MSV3drs794728250
GWAS Ctlgrs794728250
Max Magnitude0
ClinVar
Risk rs794728250(T;T)
Alt rs794728250(T;T)
Reference rs794728250(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48729205C>A
CLNSRC
CLNACC RCV000181568.2,