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rs1057517709

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517709(A;A)
Make rs1057517709(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101358348
GeneBTK
is asnp
is mentioned by
dbSNPrs1057517709
dbSNP (old)rs1057517709
ClinGenrs1057517709
ebirs1057517709
HLIrs1057517709
Exacrs1057517709
Gnomadrs1057517709
Varsomers1057517709
Maprs1057517709
PheGenIrs1057517709
Biobankrs1057517709
1000 genomesrs1057517709
hgdprs1057517709
ensemblrs1057517709
gopubmedrs1057517709
geneviewrs1057517709
scholarrs1057517709
googlers1057517709
pharmgkbrs1057517709
gwascentralrs1057517709
openSNPrs1057517709
23andMers1057517709
23andMe allrs1057517709
SNPshotrs1057517709
SNPdbers1057517709
MSV3drs1057517709
GWAS Ctlgrs1057517709
Max Magnitude0
ClinVar
Risk rs1057517709(A;A)
Alt rs1057517709(A;A)
Reference Rs1057517709(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100613336A>T
CLNSRC
CLNACC RCV000413395.1,