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rs1064796522

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTCCGCGTG;CTCCGCGTG) 0 common in clinvar
Chromosome15
Position48487317
GeneFBN1
is asnp
is mentioned by
dbSNPrs1064796522
dbSNP (old)rs1064796522
ClinGenrs1064796522
ebirs1064796522
HLIrs1064796522
Exacrs1064796522
Gnomadrs1064796522
Varsomers1064796522
Maprs1064796522
PheGenIrs1064796522
Biobankrs1064796522
1000 genomesrs1064796522
hgdprs1064796522
ensemblrs1064796522
gopubmedrs1064796522
geneviewrs1064796522
scholarrs1064796522
googlers1064796522
pharmgkbrs1064796522
gwascentralrs1064796522
openSNPrs1064796522
23andMers1064796522
23andMe allrs1064796522
SNPshotrs1064796522
SNPdbers1064796522
MSV3drs1064796522
GWAS Ctlgrs1064796522
Max Magnitude0
ClinVar
Risk rs1064796522(GTCCGCGTT;GTCCGCGTT)
Alt rs1064796522(GTCCGCGTT;GTCCGCGTT)
Reference Rs1064796522(CTCCGCGTG;CTCCGCGTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48779514_48779522delCACGCGGAGinsAACGCGGAC
CLNSRC
CLNACC RCV000480941.1,