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rs1057520682

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520682(A;A)
Make rs1057520682(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101375244
GeneBTK
is asnp
is mentioned by
dbSNPrs1057520682
dbSNP (old)rs1057520682
ClinGenrs1057520682
ebirs1057520682
HLIrs1057520682
Exacrs1057520682
Gnomadrs1057520682
Varsomers1057520682
Maprs1057520682
PheGenIrs1057520682
Biobankrs1057520682
1000 genomesrs1057520682
hgdprs1057520682
ensemblrs1057520682
gopubmedrs1057520682
geneviewrs1057520682
scholarrs1057520682
googlers1057520682
pharmgkbrs1057520682
gwascentralrs1057520682
openSNPrs1057520682
23andMers1057520682
23andMe allrs1057520682
SNPshotrs1057520682
SNPdbers1057520682
MSV3drs1057520682
GWAS Ctlgrs1057520682
Max Magnitude0
ClinVar
Risk rs1057520682(A;A)
Alt rs1057520682(A;A)
Reference Rs1057520682(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100630232G>T
CLNSRC
CLNACC RCV000425259.1,