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rs794728245

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728245(G;T)
Make rs794728245(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437830
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728245
ebirs794728245
HLIrs794728245
Exacrs794728245
Varsomers794728245
Maprs794728245
PheGenIrs794728245
hapmaprs794728245
1000 genomesrs794728245
hgdprs794728245
ensemblrs794728245
gopubmedrs794728245
geneviewrs794728245
scholarrs794728245
googlers794728245
pharmgkbrs794728245
gwascentralrs794728245
openSNPrs794728245
23andMers794728245
23andMe allrs794728245
SNP Nexus

SNPshotrs794728245
SNPdbers794728245
MSV3drs794728245
GWAS Ctlgrs794728245
Max Magnitude0
ClinVar
Risk rs794728245(T;T)
Alt rs794728245(T;T)
Reference rs794728245(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48730027C>A
CLNSRC
CLNACC RCV000181561.1,