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

rs1057521211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521211(G;T)
Make rs1057521211(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48508645
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057521211
dbSNP (classic)rs1057521211
ClinGenrs1057521211
ebirs1057521211
HLIrs1057521211
Exacrs1057521211
Gnomadrs1057521211
Varsomers1057521211
LitVarrs1057521211
Maprs1057521211
PheGenIrs1057521211
Biobankrs1057521211
1000 genomesrs1057521211
hgdprs1057521211
ensemblrs1057521211
geneviewrs1057521211
scholarrs1057521211
googlers1057521211
pharmgkbrs1057521211
gwascentralrs1057521211
openSNPrs1057521211
23andMers1057521211
SNPshotrs1057521211
SNPdbers1057521211
MSV3drs1057521211
GWAS Ctlgrs1057521211
Max Magnitude0
ClinVar
Risk rs1057521211(T;T)
Alt rs1057521211(T;T)
Reference Rs1057521211(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48800842C>A
CLNSRC
CLNACC RCV000418820.1,