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rs886041382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886041382(C;T)
Make rs886041382(T;T)
ChromosomeX
Position49078077
GeneWDR45
is asnp
is mentioned by
dbSNPrs886041382
dbSNP (classic)rs886041382
ClinGenrs886041382
ebirs886041382
HLIrs886041382
Exacrs886041382
Gnomadrs886041382
Varsomers886041382
LitVarrs886041382
Maprs886041382
PheGenIrs886041382
Biobankrs886041382
1000 genomesrs886041382
hgdprs886041382
ensemblrs886041382
geneviewrs886041382
scholarrs886041382
googlers886041382
pharmgkbrs886041382
gwascentralrs886041382
openSNPrs886041382
23andMers886041382
SNPshotrs886041382
SNPdbers886041382
MSV3drs886041382
GWAS Ctlgrs886041382
Max Magnitude0
ClinVar
Risk rs886041382(T;T)
Alt rs886041382(T;T)
Reference Rs886041382(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WDR45
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.48935736G>A
CLNSRC
CLNACC RCV000272581.1,