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rs193922416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs193922416(-;-)
Make rs193922416(-;C)
Make rs193922416(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position48688082
GeneWAS
is asnp
is mentioned by
dbSNPrs193922416
ebirs193922416
HLIrs193922416
Exacrs193922416
Varsomers193922416
Maprs193922416
PheGenIrs193922416
hapmaprs193922416
1000 genomesrs193922416
hgdprs193922416
ensemblrs193922416
gopubmedrs193922416
geneviewrs193922416
scholarrs193922416
googlers193922416
pharmgkbrs193922416
gwascentralrs193922416
openSNPrs193922416
23andMers193922416
23andMe allrs193922416
SNP Nexus

SNPshotrs193922416
SNPdbers193922416
MSV3drs193922416
GWAS Ctlgrs193922416
Max Magnitude0
ClinVar
Risk rs193922416(C;C)
Alt rs193922416(C;C)
Reference rs193922416(;)
Significance Probable-Pathogenic
Disease Wiskott-Aldrich syndrome
Variation info
Gene WAS
CLNDBN Wiskott-Aldrich syndrome
Reversed 0
HGVS NC_000023.10:g.48546471dupC
CLNSRC ClinVar LabCorp
CLNACC RCV000030597.1,