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rs1057524697

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524697(G;T)
Make rs1057524697(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48460257
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057524697
dbSNP (old)rs1057524697
ClinGenrs1057524697
ebirs1057524697
HLIrs1057524697
Exacrs1057524697
Gnomadrs1057524697
Varsomers1057524697
Maprs1057524697
PheGenIrs1057524697
Biobankrs1057524697
1000 genomesrs1057524697
hgdprs1057524697
ensemblrs1057524697
gopubmedrs1057524697
geneviewrs1057524697
scholarrs1057524697
googlers1057524697
pharmgkbrs1057524697
gwascentralrs1057524697
openSNPrs1057524697
23andMers1057524697
23andMe allrs1057524697
SNPshotrs1057524697
SNPdbers1057524697
MSV3drs1057524697
GWAS Ctlgrs1057524697
Max Magnitude0
ClinVar
Risk rs1057524697(T;T)
Alt rs1057524697(T;T)
Reference Rs1057524697(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48752454C>A
CLNSRC
CLNACC RCV000437531.1,