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rs1057515584

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057515584(-;TGTC)
Make rs1057515584(TGTC;TGTC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154352902
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057515584
dbSNP (old)rs1057515584
ClinGenrs1057515584
ebirs1057515584
HLIrs1057515584
Exacrs1057515584
Gnomadrs1057515584
Varsomers1057515584
Maprs1057515584
PheGenIrs1057515584
Biobankrs1057515584
1000 genomesrs1057515584
hgdprs1057515584
ensemblrs1057515584
gopubmedrs1057515584
geneviewrs1057515584
scholarrs1057515584
googlers1057515584
pharmgkbrs1057515584
gwascentralrs1057515584
openSNPrs1057515584
23andMers1057515584
23andMe allrs1057515584
SNPshotrs1057515584
SNPdbers1057515584
MSV3drs1057515584
GWAS Ctlgrs1057515584
Max Magnitude0
ClinVar
Risk rs1057515584(TGTC;TGTC)
Alt rs1057515584(TGTC;TGTC)
Reference Rs1057515584(-;-)
Significance Pathogenic
Disease FG syndrome 2 Intestinal pseudoobstruction neuronal chronic idiopathic X-linked
Variation info
Gene FLNA
CLNDBN FG syndrome 2 Intestinal pseudoobstruction neuronal chronic idiopathic X-linked
Reversed 1
HGVS NC_000023.10:g.153581270_153581271insGACA
CLNSRC
CLNACC RCV000341085.1, RCV000403233.1,