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rs1057521102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521102(A;A)
Make rs1057521102(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48510088
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057521102
dbSNP (old)rs1057521102
ClinGenrs1057521102
ebirs1057521102
HLIrs1057521102
Exacrs1057521102
Gnomadrs1057521102
Varsomers1057521102
Maprs1057521102
PheGenIrs1057521102
Biobankrs1057521102
1000 genomesrs1057521102
hgdprs1057521102
ensemblrs1057521102
gopubmedrs1057521102
geneviewrs1057521102
scholarrs1057521102
googlers1057521102
pharmgkbrs1057521102
gwascentralrs1057521102
openSNPrs1057521102
23andMers1057521102
23andMe allrs1057521102
SNPshotrs1057521102
SNPdbers1057521102
MSV3drs1057521102
GWAS Ctlgrs1057521102
Max Magnitude0
ClinVar
Risk rs1057521102(A;A)
Alt rs1057521102(A;A)
Reference Rs1057521102(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48802285C>T
CLNSRC
CLNACC RCV000443014.1,