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rs1057521814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521814(C;T)
Make rs1057521814(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101353923
GeneBTK
is asnp
is mentioned by
dbSNPrs1057521814
dbSNP (old)rs1057521814
ClinGenrs1057521814
ebirs1057521814
HLIrs1057521814
Exacrs1057521814
Gnomadrs1057521814
Varsomers1057521814
Maprs1057521814
PheGenIrs1057521814
Biobankrs1057521814
1000 genomesrs1057521814
hgdprs1057521814
ensemblrs1057521814
gopubmedrs1057521814
geneviewrs1057521814
scholarrs1057521814
googlers1057521814
pharmgkbrs1057521814
gwascentralrs1057521814
openSNPrs1057521814
23andMers1057521814
23andMe allrs1057521814
SNPshotrs1057521814
SNPdbers1057521814
MSV3drs1057521814
GWAS Ctlgrs1057521814
Max Magnitude0
ClinVar
Risk rs1057521814(T;T)
Alt rs1057521814(T;T)
Reference Rs1057521814(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100608911G>A
CLNSRC
CLNACC RCV000438550.1,