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rs1064794904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position101353214
GeneBTK
is asnp
is mentioned by
dbSNPrs1064794904
dbSNP (classic)rs1064794904
ClinGenrs1064794904
ebirs1064794904
HLIrs1064794904
Exacrs1064794904
Gnomadrs1064794904
Varsomers1064794904
LitVarrs1064794904
Maprs1064794904
PheGenIrs1064794904
Biobankrs1064794904
1000 genomesrs1064794904
hgdprs1064794904
ensemblrs1064794904
geneviewrs1064794904
scholarrs1064794904
googlers1064794904
pharmgkbrs1064794904
gwascentralrs1064794904
openSNPrs1064794904
23andMers1064794904
SNPshotrs1064794904
SNPdbers1064794904
MSV3drs1064794904
GWAS Ctlgrs1064794904
Max Magnitude0
ClinVar
Risk rs1064794904(C;C)
Alt rs1064794904(C;C)
Reference Rs1064794904(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100608202T>G
CLNSRC
CLNACC RCV000484290.1,