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rs1057521951

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521951(A;A)
Make rs1057521951(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position128318923
GeneFBN2
is asnp
is mentioned by
dbSNPrs1057521951
dbSNP (old)rs1057521951
ClinGenrs1057521951
ebirs1057521951
HLIrs1057521951
Exacrs1057521951
Gnomadrs1057521951
Varsomers1057521951
Maprs1057521951
PheGenIrs1057521951
Biobankrs1057521951
1000 genomesrs1057521951
hgdprs1057521951
ensemblrs1057521951
gopubmedrs1057521951
geneviewrs1057521951
scholarrs1057521951
googlers1057521951
pharmgkbrs1057521951
gwascentralrs1057521951
openSNPrs1057521951
23andMers1057521951
23andMe allrs1057521951
SNPshotrs1057521951
SNPdbers1057521951
MSV3drs1057521951
GWAS Ctlgrs1057521951
Max Magnitude0
ClinVar
Risk rs1057521951(A;A)
Alt rs1057521951(A;A)
Reference Rs1057521951(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.127654615C>T
CLNSRC
CLNACC RCV000433750.1,