rs41310709

Orientation

plus

Stabilized

plus

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

Make rs41310709(A;A)

Make rs41310709(A;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

101356112

Gene

BTK

is a	snp
is	mentioned by
dbSNP	rs41310709
dbSNP (classic)	rs41310709
ClinGen	rs41310709
ebi	rs41310709
HLI	rs41310709
Exac	rs41310709
Gnomad	rs41310709
Varsome	rs41310709
LitVar	rs41310709
Map	rs41310709
PheGenI	rs41310709
Biobank	rs41310709
1000 genomes	rs41310709
hgdp	rs41310709
ensembl	rs41310709
geneview	rs41310709
scholar	rs41310709
google	rs41310709
pharmgkb	rs41310709
gwascentral	rs41310709
openSNP	rs41310709
23andMe	rs41310709
SNPshot	rs41310709
SNPdbe	rs41310709
MSV3d	rs41310709
GWAS Ctlg	rs41310709

Max Magnitude

0

OMIM	300300
Desc
Variant	0034
Related	also

ClinVar
Risk	rs41310709(A;A) rs41310709(T;T)
Alt	rs41310709(A;A) rs41310709(T;T)
Reference	Rs41310709(G;G)
Significance	Pathogenic
Disease	X-linked agammaglobulinemia
Variation	info
Gene	BTK
CLNDBN	X-linked agammaglobulinemia
Reversed	0
HGVS	NC_000023.10:g.100611100G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012128.2,