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rs1057522908

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522908(C;C)
Make rs1057522908(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48485451
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057522908
dbSNP (old)rs1057522908
ClinGenrs1057522908
ebirs1057522908
HLIrs1057522908
Exacrs1057522908
Gnomadrs1057522908
Varsomers1057522908
Maprs1057522908
PheGenIrs1057522908
Biobankrs1057522908
1000 genomesrs1057522908
hgdprs1057522908
ensemblrs1057522908
gopubmedrs1057522908
geneviewrs1057522908
scholarrs1057522908
googlers1057522908
pharmgkbrs1057522908
gwascentralrs1057522908
openSNPrs1057522908
23andMers1057522908
23andMe allrs1057522908
SNPshotrs1057522908
SNPdbers1057522908
MSV3drs1057522908
GWAS Ctlgrs1057522908
Max Magnitude0
ClinVar
Risk rs1057522908(C;C)
Alt rs1057522908(C;C)
Reference Rs1057522908(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48777648C>G
CLNSRC
CLNACC RCV000430505.1,