Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057523406

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523406(C;C)
Make rs1057523406(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48494209
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057523406
dbSNP (old)rs1057523406
ClinGenrs1057523406
ebirs1057523406
HLIrs1057523406
Exacrs1057523406
Gnomadrs1057523406
Varsomers1057523406
Maprs1057523406
PheGenIrs1057523406
Biobankrs1057523406
1000 genomesrs1057523406
hgdprs1057523406
ensemblrs1057523406
gopubmedrs1057523406
geneviewrs1057523406
scholarrs1057523406
googlers1057523406
pharmgkbrs1057523406
gwascentralrs1057523406
openSNPrs1057523406
23andMers1057523406
23andMe allrs1057523406
SNPshotrs1057523406
SNPdbers1057523406
MSV3drs1057523406
GWAS Ctlgrs1057523406
Max Magnitude0
ClinVar
Risk rs1057523406(C;C)
Alt rs1057523406(C;C)
Reference Rs1057523406(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48786406C>G
CLNSRC
CLNACC RCV000420946.1,