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rs1057520656

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520656(A;A)
Make rs1057520656(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48520795
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057520656
dbSNP (old)rs1057520656
ClinGenrs1057520656
ebirs1057520656
HLIrs1057520656
Exacrs1057520656
Gnomadrs1057520656
Varsomers1057520656
Maprs1057520656
PheGenIrs1057520656
Biobankrs1057520656
1000 genomesrs1057520656
hgdprs1057520656
ensemblrs1057520656
gopubmedrs1057520656
geneviewrs1057520656
scholarrs1057520656
googlers1057520656
pharmgkbrs1057520656
gwascentralrs1057520656
openSNPrs1057520656
23andMers1057520656
23andMe allrs1057520656
SNPshotrs1057520656
SNPdbers1057520656
MSV3drs1057520656
GWAS Ctlgrs1057520656
Max Magnitude0
ClinVar
Risk rs1057520656(A;A)
Alt rs1057520656(A;A)
Reference Rs1057520656(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48812992G>T
CLNSRC
CLNACC RCV000422533.1,