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rs1057521116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521116(C;T)
Make rs1057521116(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101353297
GeneBTK
is asnp
is mentioned by
dbSNPrs1057521116
dbSNP (old)rs1057521116
ClinGenrs1057521116
ebirs1057521116
HLIrs1057521116
Exacrs1057521116
Gnomadrs1057521116
Varsomers1057521116
Maprs1057521116
PheGenIrs1057521116
Biobankrs1057521116
1000 genomesrs1057521116
hgdprs1057521116
ensemblrs1057521116
gopubmedrs1057521116
geneviewrs1057521116
scholarrs1057521116
googlers1057521116
pharmgkbrs1057521116
gwascentralrs1057521116
openSNPrs1057521116
23andMers1057521116
23andMe allrs1057521116
SNPshotrs1057521116
SNPdbers1057521116
MSV3drs1057521116
GWAS Ctlgrs1057521116
Max Magnitude0
ClinVar
Risk rs1057521116(T;T)
Alt rs1057521116(T;T)
Reference Rs1057521116(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100608285G>A
CLNSRC
CLNACC RCV000432214.1,