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rs1057520181

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520181(A;A)
Make rs1057520181(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48487101
GeneFBN1
is asnp
is mentioned by
dbSNPrs1057520181
dbSNP (old)rs1057520181
ClinGenrs1057520181
ebirs1057520181
HLIrs1057520181
Exacrs1057520181
Gnomadrs1057520181
Varsomers1057520181
Maprs1057520181
PheGenIrs1057520181
Biobankrs1057520181
1000 genomesrs1057520181
hgdprs1057520181
ensemblrs1057520181
gopubmedrs1057520181
geneviewrs1057520181
scholarrs1057520181
googlers1057520181
pharmgkbrs1057520181
gwascentralrs1057520181
openSNPrs1057520181
23andMers1057520181
23andMe allrs1057520181
SNPshotrs1057520181
SNPdbers1057520181
MSV3drs1057520181
GWAS Ctlgrs1057520181
Max Magnitude0
ClinVar
Risk rs1057520181(A;A)
Alt rs1057520181(A;A)
Reference Rs1057520181(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48779298G>T
CLNSRC
CLNACC RCV000427812.1,