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rs1064793636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome15
Position48497290
GeneFBN1
is asnp
is mentioned by
dbSNPrs1064793636
dbSNP (old)rs1064793636
ClinGenrs1064793636
ebirs1064793636
HLIrs1064793636
Exacrs1064793636
Gnomadrs1064793636
Varsomers1064793636
LitVarrs1064793636
Maprs1064793636
PheGenIrs1064793636
Biobankrs1064793636
1000 genomesrs1064793636
hgdprs1064793636
ensemblrs1064793636
gopubmedrs1064793636
geneviewrs1064793636
scholarrs1064793636
googlers1064793636
pharmgkbrs1064793636
gwascentralrs1064793636
openSNPrs1064793636
23andMers1064793636
23andMe allrs1064793636
SNPshotrs1064793636
SNPdbers1064793636
MSV3drs1064793636
GWAS Ctlgrs1064793636
Max Magnitude0
ClinVar
Risk rs1064793636(-;-)
Alt rs1064793636(-;-)
Reference Rs1064793636(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48789487delC
CLNSRC
CLNACC RCV000483392.1,