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rs1064796297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position154364167
GeneFLNA
is asnp
is mentioned by
dbSNPrs1064796297
dbSNP (old)rs1064796297
ClinGenrs1064796297
ebirs1064796297
HLIrs1064796297
Exacrs1064796297
Gnomadrs1064796297
Varsomers1064796297
Maprs1064796297
PheGenIrs1064796297
Biobankrs1064796297
1000 genomesrs1064796297
hgdprs1064796297
ensemblrs1064796297
gopubmedrs1064796297
geneviewrs1064796297
scholarrs1064796297
googlers1064796297
pharmgkbrs1064796297
gwascentralrs1064796297
openSNPrs1064796297
23andMers1064796297
23andMe allrs1064796297
SNPshotrs1064796297
SNPdbers1064796297
MSV3drs1064796297
GWAS Ctlgrs1064796297
Max Magnitude0
ClinVar
Risk rs1064796297(G;G)
Alt rs1064796297(G;G)
Reference Rs1064796297(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153592535T>C
CLNSRC
CLNACC RCV000482242.1,