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rs1057524757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524757(C;C)
Make rs1057524757(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48427567
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057524757
dbSNP (old)rs1057524757
ClinGenrs1057524757
ebirs1057524757
HLIrs1057524757
Exacrs1057524757
Gnomadrs1057524757
Varsomers1057524757
Maprs1057524757
PheGenIrs1057524757
Biobankrs1057524757
1000 genomesrs1057524757
hgdprs1057524757
ensemblrs1057524757
gopubmedrs1057524757
geneviewrs1057524757
scholarrs1057524757
googlers1057524757
pharmgkbrs1057524757
gwascentralrs1057524757
openSNPrs1057524757
23andMers1057524757
23andMe allrs1057524757
SNPshotrs1057524757
SNPdbers1057524757
MSV3drs1057524757
GWAS Ctlgrs1057524757
Max Magnitude0
ClinVar
Risk rs1057524757(C;C)
Alt rs1057524757(C;C)
Reference Rs1057524757(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48719764C>G
CLNSRC
CLNACC RCV000418336.1,