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rs886039308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039308(A;A)
Make rs886039308(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position25013006
GeneARX
is asnp
is mentioned by
dbSNPrs886039308
dbSNP (classic)rs886039308
ClinGenrs886039308
ebirs886039308
HLIrs886039308
Exacrs886039308
Gnomadrs886039308
Varsomers886039308
LitVarrs886039308
Maprs886039308
PheGenIrs886039308
Biobankrs886039308
1000 genomesrs886039308
hgdprs886039308
ensemblrs886039308
geneviewrs886039308
scholarrs886039308
googlers886039308
pharmgkbrs886039308
gwascentralrs886039308
openSNPrs886039308
23andMers886039308
23andMe allrs886039308
SNPshotrs886039308
SNPdbers886039308
MSV3drs886039308
GWAS Ctlgrs886039308
Max Magnitude0
ClinVar
Risk rs886039308(A;A)
Alt rs886039308(A;A)
Reference Rs886039308(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25031123C>T
CLNSRC
CLNACC RCV000255677.2,