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

rs1057521103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521103(C;C)
Make rs1057521103(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48596360
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057521103
dbSNP (classic)rs1057521103
ClinGenrs1057521103
ebirs1057521103
HLIrs1057521103
Exacrs1057521103
Gnomadrs1057521103
Varsomers1057521103
LitVarrs1057521103
Maprs1057521103
PheGenIrs1057521103
Biobankrs1057521103
1000 genomesrs1057521103
hgdprs1057521103
ensemblrs1057521103
geneviewrs1057521103
scholarrs1057521103
googlers1057521103
pharmgkbrs1057521103
gwascentralrs1057521103
openSNPrs1057521103
23andMers1057521103
23andMe allrs1057521103
SNPshotrs1057521103
SNPdbers1057521103
MSV3drs1057521103
GWAS Ctlgrs1057521103
Max Magnitude0
ClinVar
Risk rs1057521103(C;C)
Alt rs1057521103(C;C)
Reference Rs1057521103(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48888557C>G
CLNSRC
CLNACC RCV000433676.1,