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rs1057523796

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523796(A;A)
Make rs1057523796(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48472677
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057523796
dbSNP (old)rs1057523796
ClinGenrs1057523796
ebirs1057523796
HLIrs1057523796
Exacrs1057523796
Gnomadrs1057523796
Varsomers1057523796
Maprs1057523796
PheGenIrs1057523796
Biobankrs1057523796
1000 genomesrs1057523796
hgdprs1057523796
ensemblrs1057523796
gopubmedrs1057523796
geneviewrs1057523796
scholarrs1057523796
googlers1057523796
pharmgkbrs1057523796
gwascentralrs1057523796
openSNPrs1057523796
23andMers1057523796
23andMe allrs1057523796
SNPshotrs1057523796
SNPdbers1057523796
MSV3drs1057523796
GWAS Ctlgrs1057523796
Max Magnitude0
ClinVar
Risk rs1057523796(A;A)
Alt rs1057523796(A;A)
Reference Rs1057523796(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48764874C>T
CLNSRC
CLNACC RCV000424708.1,