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rs1057521859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521859(C;T)
Make rs1057521859(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48513615
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057521859
dbSNP (classic)rs1057521859
ClinGenrs1057521859
ebirs1057521859
HLIrs1057521859
Exacrs1057521859
Gnomadrs1057521859
Varsomers1057521859
LitVarrs1057521859
Maprs1057521859
PheGenIrs1057521859
Biobankrs1057521859
1000 genomesrs1057521859
hgdprs1057521859
ensemblrs1057521859
geneviewrs1057521859
scholarrs1057521859
googlers1057521859
pharmgkbrs1057521859
gwascentralrs1057521859
openSNPrs1057521859
23andMers1057521859
23andMe allrs1057521859
SNPshotrs1057521859
SNPdbers1057521859
MSV3drs1057521859
GWAS Ctlgrs1057521859
Max Magnitude0
ClinVar
Risk rs1057521859(T;T)
Alt rs1057521859(T;T)
Reference Rs1057521859(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48805812G>A
CLNSRC
CLNACC RCV000430329.1,