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rs1057520578

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520578(C;C)
Make rs1057520578(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101354681
GeneBTK
is asnp
is mentioned by
dbSNPrs1057520578
dbSNP (old)rs1057520578
ClinGenrs1057520578
ebirs1057520578
HLIrs1057520578
Exacrs1057520578
Gnomadrs1057520578
Varsomers1057520578
Maprs1057520578
PheGenIrs1057520578
Biobankrs1057520578
1000 genomesrs1057520578
hgdprs1057520578
ensemblrs1057520578
gopubmedrs1057520578
geneviewrs1057520578
scholarrs1057520578
googlers1057520578
pharmgkbrs1057520578
gwascentralrs1057520578
openSNPrs1057520578
23andMers1057520578
23andMe allrs1057520578
SNPshotrs1057520578
SNPdbers1057520578
MSV3drs1057520578
GWAS Ctlgrs1057520578
Max Magnitude0
ClinVar
Risk rs1057520578(C;C)
Alt rs1057520578(C;C)
Reference Rs1057520578(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100609669C>G
CLNSRC
CLNACC RCV000435923.1,