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rs587776742

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776742(A;T)
Make rs587776742(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position48683854
GeneWAS
is asnp
is mentioned by
dbSNPrs587776742
ebirs587776742
HLIrs587776742
Exacrs587776742
Varsomers587776742
Maprs587776742
PheGenIrs587776742
hapmaprs587776742
1000 genomesrs587776742
hgdprs587776742
ensemblrs587776742
gopubmedrs587776742
geneviewrs587776742
scholarrs587776742
googlers587776742
pharmgkbrs587776742
gwascentralrs587776742
openSNPrs587776742
23andMers587776742
23andMe allrs587776742
SNP Nexus

SNPshotrs587776742
SNPdbers587776742
MSV3drs587776742
GWAS Ctlgrs587776742
Max Magnitude0
ClinVar
Risk rs587776742(T;T)
Alt rs587776742(T;T)
Reference rs587776742(A;A)
Significance Pathogenic
Disease Wiskott-Aldrich syndrome
Variation info
Gene WAS
CLNDBN Wiskott-Aldrich syndrome
Reversed 0
HGVS NC_000023.10:g.48542243A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011869.4,