Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057521100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521100(G;T)
Make rs1057521100(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48415585
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057521100
dbSNP (old)rs1057521100
ClinGenrs1057521100
ebirs1057521100
HLIrs1057521100
Exacrs1057521100
Gnomadrs1057521100
Varsomers1057521100
Maprs1057521100
PheGenIrs1057521100
Biobankrs1057521100
1000 genomesrs1057521100
hgdprs1057521100
ensemblrs1057521100
gopubmedrs1057521100
geneviewrs1057521100
scholarrs1057521100
googlers1057521100
pharmgkbrs1057521100
gwascentralrs1057521100
openSNPrs1057521100
23andMers1057521100
23andMe allrs1057521100
SNPshotrs1057521100
SNPdbers1057521100
MSV3drs1057521100
GWAS Ctlgrs1057521100
Max Magnitude0
ClinVar
Risk rs1057521100(T;T)
Alt rs1057521100(T;T)
Reference Rs1057521100(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48707782C>A
CLNSRC
CLNACC RCV000424126.1,