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

rs1057515582

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057515582(-;AA)
Make rs1057515582(AA;AA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154362725
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057515582
dbSNP (old)rs1057515582
ClinGenrs1057515582
ebirs1057515582
HLIrs1057515582
Exacrs1057515582
Gnomadrs1057515582
Varsomers1057515582
Maprs1057515582
PheGenIrs1057515582
Biobankrs1057515582
1000 genomesrs1057515582
hgdprs1057515582
ensemblrs1057515582
gopubmedrs1057515582
geneviewrs1057515582
scholarrs1057515582
googlers1057515582
pharmgkbrs1057515582
gwascentralrs1057515582
openSNPrs1057515582
23andMers1057515582
23andMe allrs1057515582
SNPshotrs1057515582
SNPdbers1057515582
MSV3drs1057515582
GWAS Ctlgrs1057515582
Max Magnitude0
ClinVar
Risk rs1057515582(AA;AA)
Alt rs1057515582(AA;AA)
Reference Rs1057515582(-;-)
Significance Pathogenic
Disease Periventricular nodular heterotopia 1
Variation info
Gene FLNA
CLNDBN Periventricular nodular heterotopia 1
Reversed 1
HGVS NC_000023.10:g.153591093_153591094insTT
CLNSRC
CLNACC RCV000348703.1,