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rs886041693

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886041693(A;G)
Make rs886041693(G;G)
ChromosomeX
Position49075947
GenePRAF2, WDR45
is asnp
is mentioned by
dbSNPrs886041693
dbSNP (classic)rs886041693
ClinGenrs886041693
ebirs886041693
HLIrs886041693
Exacrs886041693
Gnomadrs886041693
Varsomers886041693
LitVarrs886041693
Maprs886041693
PheGenIrs886041693
Biobankrs886041693
1000 genomesrs886041693
hgdprs886041693
ensemblrs886041693
geneviewrs886041693
scholarrs886041693
googlers886041693
pharmgkbrs886041693
gwascentralrs886041693
openSNPrs886041693
23andMers886041693
SNPshotrs886041693
SNPdbers886041693
MSV3drs886041693
GWAS Ctlgrs886041693
Max Magnitude0
ClinVar
Risk rs886041693(G;G)
Alt rs886041693(G;G)
Reference Rs886041693(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene WDR45 PRAF2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.48933606T>C
CLNSRC
CLNACC RCV000380857.1,