rs886039321

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs886039321(C;C)

Make rs886039321(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

101353342

Gene

BTK

is a	snp
is	mentioned by
dbSNP	rs886039321
dbSNP (classic)	rs886039321
ClinGen	rs886039321
ebi	rs886039321
HLI	rs886039321
Exac	rs886039321
Gnomad	rs886039321
Varsome	rs886039321
LitVar	rs886039321
Map	rs886039321
PheGenI	rs886039321
Biobank	rs886039321
1000 genomes	rs886039321
hgdp	rs886039321
ensembl	rs886039321
geneview	rs886039321
scholar	rs886039321
google	rs886039321
pharmgkb	rs886039321
gwascentral	rs886039321
openSNP	rs886039321
23andMe	rs886039321
SNPshot	rs886039321
SNPdbe	rs886039321
MSV3d	rs886039321
GWAS Ctlg	rs886039321

Max Magnitude

0

ClinVar
Risk	rs886039321(C;C)
Alt	rs886039321(C;C)
Reference	Rs886039321(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BTK
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.100608330A>G
CLNSRC
CLNACC	RCV000255772.1,