rs128621199

Orientation

minus

Stabilized

minus

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

Make rs128621199(A;A)

Make rs128621199(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

101356858

Gene

BTK

is a	snp
is	mentioned by
dbSNP	rs128621199
dbSNP (classic)	rs128621199
ClinGen	rs128621199
ebi	rs128621199
HLI	rs128621199
Exac	rs128621199
Gnomad	rs128621199
Varsome	rs128621199
LitVar	rs128621199
Map	rs128621199
PheGenI	rs128621199
Biobank	rs128621199
1000 genomes	rs128621199
hgdp	rs128621199
ensembl	rs128621199
geneview	rs128621199
scholar	rs128621199
google	rs128621199
pharmgkb	rs128621199
gwascentral	rs128621199
openSNP	rs128621199
23andMe	rs128621199
SNPshot	rs128621199
SNPdbe	rs128621199
MSV3d	rs128621199
GWAS Ctlg	rs128621199

Max Magnitude

0

OMIM	300300
Desc
Variant	0033
Related	also

ClinVar
Risk	rs128621199(A;A) rs128621199(T;T)
Alt	rs128621199(A;A) rs128621199(T;T)
Reference	Rs128621199(C;C)
Significance	Pathogenic
Disease	X-linked agammaglobulinemia
Variation	info
Gene	BTK
CLNDBN	X-linked agammaglobulinemia
Reversed	1
HGVS	NC_000023.10:g.100611846G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012127.17,