rs35062843

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs35062843(G;G)

Make rs35062843(G;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

16948892

Gene

TNFRSF13B

is a	snp
is	mentioned by
dbSNP	rs35062843
dbSNP (classic)	rs35062843
ClinGen	rs35062843
ebi	rs35062843
HLI	rs35062843
Exac	rs35062843
Gnomad	rs35062843
Varsome	rs35062843
LitVar	rs35062843
Map	rs35062843
PheGenI	rs35062843
Biobank	rs35062843
1000 genomes	rs35062843
hgdp	rs35062843
ensembl	rs35062843
geneview	rs35062843
scholar	rs35062843
google	rs35062843
pharmgkb	rs35062843
gwascentral	rs35062843
openSNP	rs35062843
23andMe	rs35062843
SNPshot	rs35062843
SNPdbe	rs35062843
MSV3d	rs35062843
GWAS Ctlg	rs35062843

GMAF

0.02801

Max Magnitude

0

[PMID 19775471] Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8

ClinVar
Risk	rs35062843(G;G)
Alt	rs35062843(G;G)
Reference	Rs35062843(T;T)
Significance	Probable-non-pathogenic
Disease	not specified Common Variable Immune Deficiency
Variation	info
Gene	TNFRSF13B
CLNDBN	not specified Common Variable Immune Deficiency, Dominant
Reversed	1
HGVS	NC_000017.10:g.16852206A>C
CLNSRC
CLNACC	RCV000252622.1, RCV000359099.1,