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rs587776745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776745(-;-)
Make rs587776745(-;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position48683864
GeneWAS
is asnp
is mentioned by
dbSNPrs587776745
ebirs587776745
HLIrs587776745
Exacrs587776745
Varsomers587776745
Maprs587776745
PheGenIrs587776745
hapmaprs587776745
1000 genomesrs587776745
hgdprs587776745
ensemblrs587776745
gopubmedrs587776745
geneviewrs587776745
scholarrs587776745
googlers587776745
pharmgkbrs587776745
gwascentralrs587776745
openSNPrs587776745
23andMers587776745
23andMe allrs587776745
SNP Nexus

SNPshotrs587776745
SNPdbers587776745
MSV3drs587776745
GWAS Ctlgrs587776745
Max Magnitude0
ClinVar
Risk rs587776745(;)
Alt rs587776745(;)
Reference rs587776745(G;G)
Significance Pathogenic
Disease Wiskott-Aldrich syndrome
Variation info
Gene WAS
CLNDBN Wiskott-Aldrich syndrome
Reversed 0
HGVS NC_000023.10:g.48542253delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000011882.5,