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rs864321663

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321663(A;G)
Make rs864321663(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101370081
GeneBTK
is asnp
is mentioned by
dbSNPrs864321663
ebirs864321663
HLIrs864321663
Exacrs864321663
Varsomers864321663
Maprs864321663
PheGenIrs864321663
hapmaprs864321663
1000 genomesrs864321663
hgdprs864321663
ensemblrs864321663
gopubmedrs864321663
geneviewrs864321663
scholarrs864321663
googlers864321663
pharmgkbrs864321663
gwascentralrs864321663
openSNPrs864321663
23andMers864321663
23andMe allrs864321663
SNP Nexus

SNPshotrs864321663
SNPdbers864321663
MSV3drs864321663
GWAS Ctlgrs864321663
Max Magnitude0
ClinVar
Risk rs864321663(G;G)
Alt rs864321663(G;G)
Reference rs864321663(A;A)
Significance Pathogenic
Disease X-linked agammaglobulinemia
Variation info
Gene BTK
CLNDBN X-linked agammaglobulinemia
Reversed 1
HGVS NC_000023.10:g.100625069T>C
CLNSRC BTK @ LOVD OMIM Allelic Variant
CLNACC RCV000012108.11,