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rs1057518023

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518023(G;T)
Make rs1057518023(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48411331
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057518023
dbSNP (old)rs1057518023
ClinGenrs1057518023
ebirs1057518023
HLIrs1057518023
Exacrs1057518023
Gnomadrs1057518023
Varsomers1057518023
Maprs1057518023
PheGenIrs1057518023
Biobankrs1057518023
1000 genomesrs1057518023
hgdprs1057518023
ensemblrs1057518023
gopubmedrs1057518023
geneviewrs1057518023
scholarrs1057518023
googlers1057518023
pharmgkbrs1057518023
gwascentralrs1057518023
openSNPrs1057518023
23andMers1057518023
23andMe allrs1057518023
SNPshotrs1057518023
SNPdbers1057518023
MSV3drs1057518023
GWAS Ctlgrs1057518023
Max Magnitude0
ClinVar
Risk rs1057518023(T;T)
Alt rs1057518023(T;T)
Reference Rs1057518023(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48703528C>A
CLNSRC
CLNACC RCV000413001.1,