rs128621191

Orientation

minus

Stabilized

minus

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

Make rs128621191(G;T)

Make rs128621191(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

101360626

Gene

BTK

is a	snp
is	mentioned by
dbSNP	rs128621191
dbSNP (classic)	rs128621191
ClinGen	rs128621191
ebi	rs128621191
HLI	rs128621191
Exac	rs128621191
Gnomad	rs128621191
Varsome	rs128621191
LitVar	rs128621191
Map	rs128621191
PheGenI	rs128621191
Biobank	rs128621191
1000 genomes	rs128621191
hgdp	rs128621191
ensembl	rs128621191
geneview	rs128621191
scholar	rs128621191
google	rs128621191
pharmgkb	rs128621191
gwascentral	rs128621191
openSNP	rs128621191
23andMe	rs128621191
SNPshot	rs128621191
SNPdbe	rs128621191
MSV3d	rs128621191
GWAS Ctlg	rs128621191

Max Magnitude

0

OMIM	300300
Desc
Variant	0020
Related	also

ClinVar
Risk	rs128621191(T;T)
Alt	rs128621191(T;T)
Reference	Rs128621191(G;G)
Significance	Pathogenic
Disease	X-linked agammaglobulinemia
Variation	info
Gene	BTK
CLNDBN	X-linked agammaglobulinemia
Reversed	1
HGVS	NC_000023.10:g.100615614C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012114.2,