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rs1064796667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome15
Position48420736
GeneFBN1
is asnp
is mentioned by
dbSNPrs1064796667
dbSNP (classic)rs1064796667
ClinGenrs1064796667
ebirs1064796667
HLIrs1064796667
Exacrs1064796667
Gnomadrs1064796667
Varsomers1064796667
LitVarrs1064796667
Maprs1064796667
PheGenIrs1064796667
Biobankrs1064796667
1000 genomesrs1064796667
hgdprs1064796667
ensemblrs1064796667
geneviewrs1064796667
scholarrs1064796667
googlers1064796667
pharmgkbrs1064796667
gwascentralrs1064796667
openSNPrs1064796667
23andMers1064796667
23andMe allrs1064796667
SNPshotrs1064796667
SNPdbers1064796667
MSV3drs1064796667
GWAS Ctlgrs1064796667
Max Magnitude0
ClinVar
Risk rs1064796667(G;G)
Alt rs1064796667(G;G)
Reference Rs1064796667(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48712933G>C
CLNSRC
CLNACC RCV000487148.1,