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rs1057520612

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520612(A;A)
Make rs1057520612(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101360675
GeneBTK
is asnp
is mentioned by
dbSNPrs1057520612
dbSNP (old)rs1057520612
ClinGenrs1057520612
ebirs1057520612
HLIrs1057520612
Exacrs1057520612
Gnomadrs1057520612
Varsomers1057520612
Maprs1057520612
PheGenIrs1057520612
Biobankrs1057520612
1000 genomesrs1057520612
hgdprs1057520612
ensemblrs1057520612
gopubmedrs1057520612
geneviewrs1057520612
scholarrs1057520612
googlers1057520612
pharmgkbrs1057520612
gwascentralrs1057520612
openSNPrs1057520612
23andMers1057520612
23andMe allrs1057520612
SNPshotrs1057520612
SNPdbers1057520612
MSV3drs1057520612
GWAS Ctlgrs1057520612
Max Magnitude0
ClinVar
Risk rs1057520612(A;A)
Alt rs1057520612(A;A)
Reference Rs1057520612(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100615663A>T
CLNSRC
CLNACC RCV000424404.1,