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rs193922132

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922132(A;G)
Make rs193922132(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101358698
GeneBTK
is asnp
is mentioned by
dbSNPrs193922132
ebirs193922132
HLIrs193922132
Exacrs193922132
Varsomers193922132
Maprs193922132
PheGenIrs193922132
hapmaprs193922132
1000 genomesrs193922132
hgdprs193922132
ensemblrs193922132
gopubmedrs193922132
geneviewrs193922132
scholarrs193922132
googlers193922132
pharmgkbrs193922132
gwascentralrs193922132
openSNPrs193922132
23andMers193922132
23andMe allrs193922132
SNP Nexus

SNPshotrs193922132
SNPdbers193922132
MSV3drs193922132
GWAS Ctlgrs193922132
Max Magnitude0
ClinVar
Risk rs193922132(G;G)
Alt rs193922132(G;G)
Reference rs193922132(A;A)
Significance Probable-Pathogenic
Disease X-linked agammaglobulinemia
Variation info
Gene BTK
CLNDBN X-linked agammaglobulinemia
Reversed 1
HGVS NC_000023.10:g.100613686T>C
CLNSRC ClinVar
CLNACC RCV000029417.1,