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rs1057517851

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs1057517851(-;-)
Make rs1057517851(-;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48441764
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057517851
dbSNP (old)rs1057517851
ClinGenrs1057517851
ebirs1057517851
HLIrs1057517851
Exacrs1057517851
Gnomadrs1057517851
Varsomers1057517851
Maprs1057517851
PheGenIrs1057517851
Biobankrs1057517851
1000 genomesrs1057517851
hgdprs1057517851
ensemblrs1057517851
gopubmedrs1057517851
geneviewrs1057517851
scholarrs1057517851
googlers1057517851
pharmgkbrs1057517851
gwascentralrs1057517851
openSNPrs1057517851
23andMers1057517851
23andMe allrs1057517851
SNPshotrs1057517851
SNPdbers1057517851
MSV3drs1057517851
GWAS Ctlgrs1057517851
Max Magnitude0
ClinVar
Risk rs1057517851(-;-)
Alt rs1057517851(-;-)
Reference Rs1057517851(GT;GT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48733961_48733962delAC
CLNSRC
CLNACC RCV000413502.1,