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rs794728244

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728244(A;T)
Make rs794728244(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437919
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728244
ebirs794728244
HLIrs794728244
Exacrs794728244
Varsomers794728244
Maprs794728244
PheGenIrs794728244
hapmaprs794728244
1000 genomesrs794728244
hgdprs794728244
ensemblrs794728244
gopubmedrs794728244
geneviewrs794728244
scholarrs794728244
googlers794728244
pharmgkbrs794728244
gwascentralrs794728244
openSNPrs794728244
23andMers794728244
23andMe allrs794728244
SNP Nexus

SNPshotrs794728244
SNPdbers794728244
MSV3drs794728244
GWAS Ctlgrs794728244
Max Magnitude0
ClinVar
Risk rs794728244(T;T)
Alt rs794728244(T;T)
Reference rs794728244(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48730116T>A
CLNSRC
CLNACC RCV000181558.2,