Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796581

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position154362334
GeneFLNA
is asnp
is mentioned by
dbSNPrs1064796581
dbSNP (old)rs1064796581
ClinGenrs1064796581
ebirs1064796581
HLIrs1064796581
Exacrs1064796581
Gnomadrs1064796581
Varsomers1064796581
Maprs1064796581
PheGenIrs1064796581
Biobankrs1064796581
1000 genomesrs1064796581
hgdprs1064796581
ensemblrs1064796581
gopubmedrs1064796581
geneviewrs1064796581
scholarrs1064796581
googlers1064796581
pharmgkbrs1064796581
gwascentralrs1064796581
openSNPrs1064796581
23andMers1064796581
23andMe allrs1064796581
SNPshotrs1064796581
SNPdbers1064796581
MSV3drs1064796581
GWAS Ctlgrs1064796581
Max Magnitude0
ClinVar
Risk rs1064796581(G;G)
Alt rs1064796581(G;G)
Reference Rs1064796581(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153590702T>C
CLNSRC
CLNACC RCV000483054.1,