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rs1057522902

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522902(G;T)
Make rs1057522902(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48470711
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057522902
dbSNP (old)rs1057522902
ClinGenrs1057522902
ebirs1057522902
HLIrs1057522902
Exacrs1057522902
Gnomadrs1057522902
Varsomers1057522902
Maprs1057522902
PheGenIrs1057522902
Biobankrs1057522902
1000 genomesrs1057522902
hgdprs1057522902
ensemblrs1057522902
gopubmedrs1057522902
geneviewrs1057522902
scholarrs1057522902
googlers1057522902
pharmgkbrs1057522902
gwascentralrs1057522902
openSNPrs1057522902
23andMers1057522902
23andMe allrs1057522902
SNPshotrs1057522902
SNPdbers1057522902
MSV3drs1057522902
GWAS Ctlgrs1057522902
Max Magnitude0
ClinVar
Risk rs1057522902(T;T)
Alt rs1057522902(T;T)
Reference Rs1057522902(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48762908C>A; NC_000015.9:g.48762908C>G
CLNSRC
CLNACC RCV000428134.1, RCV000494061.1,