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rs1057517855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517855(A;A)
Make rs1057517855(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48441798
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057517855
dbSNP (classic)rs1057517855
ClinGenrs1057517855
ebirs1057517855
HLIrs1057517855
Exacrs1057517855
Gnomadrs1057517855
Varsomers1057517855
LitVarrs1057517855
Maprs1057517855
PheGenIrs1057517855
Biobankrs1057517855
1000 genomesrs1057517855
hgdprs1057517855
ensemblrs1057517855
geneviewrs1057517855
scholarrs1057517855
googlers1057517855
pharmgkbrs1057517855
gwascentralrs1057517855
openSNPrs1057517855
23andMers1057517855
23andMe allrs1057517855
SNPshotrs1057517855
SNPdbers1057517855
MSV3drs1057517855
GWAS Ctlgrs1057517855
Max Magnitude0
ClinVar
Risk rs1057517855(A;A)
Alt rs1057517855(A;A)
Reference Rs1057517855(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48733995C>T
CLNSRC
CLNACC RCV000413542.1,