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rs1064793859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position101359292
GeneBTK
is asnp
is mentioned by
dbSNPrs1064793859
dbSNP (classic)rs1064793859
ClinGenrs1064793859
ebirs1064793859
HLIrs1064793859
Exacrs1064793859
Gnomadrs1064793859
Varsomers1064793859
LitVarrs1064793859
Maprs1064793859
PheGenIrs1064793859
Biobankrs1064793859
1000 genomesrs1064793859
hgdprs1064793859
ensemblrs1064793859
geneviewrs1064793859
scholarrs1064793859
googlers1064793859
pharmgkbrs1064793859
gwascentralrs1064793859
openSNPrs1064793859
23andMers1064793859
SNPshotrs1064793859
SNPdbers1064793859
MSV3drs1064793859
GWAS Ctlgrs1064793859
Max Magnitude0
ClinVar
Risk rs1064793859(A;A)
Alt rs1064793859(A;A)
Reference Rs1064793859(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100614280C>T
CLNSRC
CLNACC RCV000480016.1,