Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517710

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517710(A;A)
Make rs1057517710(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position101357583
GeneBTK
is asnp
is mentioned by
dbSNPrs1057517710
dbSNP (classic)rs1057517710
ClinGenrs1057517710
ebirs1057517710
HLIrs1057517710
Exacrs1057517710
Gnomadrs1057517710
Varsomers1057517710
LitVarrs1057517710
Maprs1057517710
PheGenIrs1057517710
Biobankrs1057517710
1000 genomesrs1057517710
hgdprs1057517710
ensemblrs1057517710
geneviewrs1057517710
scholarrs1057517710
googlers1057517710
pharmgkbrs1057517710
gwascentralrs1057517710
openSNPrs1057517710
23andMers1057517710
23andMe allrs1057517710
SNPshotrs1057517710
SNPdbers1057517710
MSV3drs1057517710
GWAS Ctlgrs1057517710
Max Magnitude0
ClinVar
Risk rs1057517710(A;A)
Alt rs1057517710(A;A)
Reference Rs1057517710(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100612571C>T
CLNSRC
CLNACC RCV000414003.1,