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rs1064796836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position101356948
GeneBTK
is asnp
is mentioned by
dbSNPrs1064796836
dbSNP (old)rs1064796836
ClinGenrs1064796836
ebirs1064796836
HLIrs1064796836
Exacrs1064796836
Gnomadrs1064796836
Varsomers1064796836
Maprs1064796836
PheGenIrs1064796836
Biobankrs1064796836
1000 genomesrs1064796836
hgdprs1064796836
ensemblrs1064796836
gopubmedrs1064796836
geneviewrs1064796836
scholarrs1064796836
googlers1064796836
pharmgkbrs1064796836
gwascentralrs1064796836
openSNPrs1064796836
23andMers1064796836
23andMe allrs1064796836
SNPshotrs1064796836
SNPdbers1064796836
MSV3drs1064796836
GWAS Ctlgrs1064796836
Max Magnitude0
ClinVar
Risk rs1064796836(A;A)
Alt rs1064796836(A;A)
Reference Rs1064796836(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene BTK
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.100611936C>T
CLNSRC
CLNACC RCV000485824.1,