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rs41310709

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common
Make rs41310709(A;A)
Make rs41310709(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position101356112
GeneBTK
is asnp
is mentioned by
dbSNPrs41310709
ebirs41310709
HLIrs41310709
Exacrs41310709
Varsomers41310709
Maprs41310709
PheGenIrs41310709
hapmaprs41310709
1000 genomesrs41310709
hgdprs41310709
ensemblrs41310709
gopubmedrs41310709
geneviewrs41310709
scholarrs41310709
googlers41310709
pharmgkbrs41310709
gwascentralrs41310709
openSNPrs41310709
23andMers41310709
23andMe allrs41310709
SNP Nexus

SNPshotrs41310709
SNPdbers41310709
MSV3drs41310709
GWAS Ctlgrs41310709
Max Magnitude0
OMIM300300
Desc
Variant0034
Relatedalso


ClinVar
Risk rs41310709(A,T;A,T)
Alt rs41310709(A,T;A,T)
Reference rs41310709(G;G)
Significance Pathogenic
Disease X-linked agammaglobulinemia
Variation info
Gene BTK
CLNDBN X-linked agammaglobulinemia
Reversed 0
HGVS NC_000023.10:g.100611100G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012128.2,