rs34562254

Orientation

minus

Stabilized

minus

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

Make rs34562254(C;T)

Make rs34562254(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

16939677

Gene

TNFRSF13B

is a	snp
is	mentioned by
dbSNP	rs34562254
dbSNP (classic)	rs34562254
ClinGen	rs34562254
ebi	rs34562254
HLI	rs34562254
Exac	rs34562254
Gnomad	rs34562254
Varsome	rs34562254
LitVar	rs34562254
Map	rs34562254
PheGenI	rs34562254
Biobank	rs34562254
1000 genomes	rs34562254
hgdp	rs34562254
ensembl	rs34562254
geneview	rs34562254
scholar	rs34562254
google	rs34562254
pharmgkb	rs34562254
gwascentral	rs34562254
openSNP	rs34562254
23andMe	rs34562254
SNPshot	rs34562254
SNPdbe	rs34562254
MSV3d	rs34562254
GWAS Ctlg	rs34562254

Max Magnitude

0

ClinVar
Risk	rs34562254(T;T)
Alt	rs34562254(T;T)
Reference	Rs34562254(C;C)
Significance	Non-pathogenic
Disease	Common Variable Immune Deficiency not specified
Variation	info
Gene	TNFRSF13B
CLNDBN	Common Variable Immune Deficiency, Dominant not specified
Reversed	1
HGVS	NC_000017.10:g.16842991G>A
CLNSRC
CLNACC	RCV000312789.1, RCV000455556.1,