rs34557412

Orientation

minus

Stabilized

minus

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

Make rs34557412(C;C)

Make rs34557412(C;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

16948873

Gene

TNFRSF13B

is a	snp
is	mentioned by
dbSNP	rs34557412
dbSNP (classic)	rs34557412
ClinGen	rs34557412
ebi	rs34557412
HLI	rs34557412
Exac	rs34557412
Gnomad	rs34557412
Varsome	rs34557412
LitVar	rs34557412
Map	rs34557412
PheGenI	rs34557412
Biobank	rs34557412
1000 genomes	rs34557412
hgdp	rs34557412
ensembl	rs34557412
geneview	rs34557412
scholar	rs34557412
google	rs34557412
pharmgkb	rs34557412
gwascentral	rs34557412
openSNP	rs34557412
23andMe	rs34557412
SNPshot	rs34557412
SNPdbe	rs34557412
MSV3d	rs34557412
GWAS Ctlg	rs34557412

GMAF

0.003214

Max Magnitude

0

OMIM	604907
Desc
Variant	0001
Related	also

ClinVar
Risk	rs34557412(C;C)
Alt	rs34557412(C;C)
Reference	Rs34557412(T;T)
Significance	Other
Disease	Common variable immunodeficiency 2 Immunoglobulin A deficiency 2 Common Variable Immune Deficiency not provided
Variation	info
Gene	TNFRSF13B
CLNDBN	Common variable immunodeficiency 2 Immunoglobulin A deficiency 2 Common Variable Immune Deficiency, Dominant not provided
Reversed	1
HGVS	NC_000017.10:g.16852187A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005623.2, RCV000005624.2, RCV000302082.1, RCV000403933.1,