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rs587776744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776744(-;-)
Make rs587776744(-;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position48688825
GeneWAS
is asnp
is mentioned by
dbSNPrs587776744
ebirs587776744
HLIrs587776744
Exacrs587776744
Varsomers587776744
Maprs587776744
PheGenIrs587776744
hapmaprs587776744
1000 genomesrs587776744
hgdprs587776744
ensemblrs587776744
gopubmedrs587776744
geneviewrs587776744
scholarrs587776744
googlers587776744
pharmgkbrs587776744
gwascentralrs587776744
openSNPrs587776744
23andMers587776744
23andMe allrs587776744
SNP Nexus

SNPshotrs587776744
SNPdbers587776744
MSV3drs587776744
GWAS Ctlgrs587776744
Max Magnitude0
ClinVar
Risk rs587776744(;)
Alt rs587776744(;)
Reference rs587776744(G;G)
Significance Pathogenic
Disease Wiskott-Aldrich syndrome
Variation info
Gene WAS
CLNDBN Wiskott-Aldrich syndrome
Reversed 0
HGVS NC_000023.10:g.48547214delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000011873.6,