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rs864321662

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321662(C;C)
Make rs864321662(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101370080
GeneBTK
is asnp
is mentioned by
dbSNPrs864321662
ebirs864321662
HLIrs864321662
Exacrs864321662
Varsomers864321662
Maprs864321662
PheGenIrs864321662
hapmaprs864321662
1000 genomesrs864321662
hgdprs864321662
ensemblrs864321662
gopubmedrs864321662
geneviewrs864321662
scholarrs864321662
googlers864321662
pharmgkbrs864321662
gwascentralrs864321662
openSNPrs864321662
23andMers864321662
23andMe allrs864321662
SNP Nexus

SNPshotrs864321662
SNPdbers864321662
MSV3drs864321662
GWAS Ctlgrs864321662
Max Magnitude0
ClinVar
Risk rs864321662(C;C)
Alt rs864321662(C;C)
Reference rs864321662(G;G)
Significance Pathogenic
Disease X-linked agammaglobulinemia
Variation info
Gene BTK
CLNDBN X-linked agammaglobulinemia
Reversed 1
HGVS NC_000023.10:g.100625068C>G
CLNSRC BTK @ LOVD OMIM Allelic Variant
CLNACC RCV000012107.11,