rs104894650

Orientation

minus

Stabilized

minus

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

Make rs104894650(A;A)

Make rs104894650(A;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

16948752

Gene

TNFRSF13B

is a	snp
is	mentioned by
dbSNP	rs104894650
dbSNP (classic)	rs104894650
ClinGen	rs104894650
ebi	rs104894650
HLI	rs104894650
Exac	rs104894650
Gnomad	rs104894650
Varsome	rs104894650
LitVar	rs104894650
Map	rs104894650
PheGenI	rs104894650
Biobank	rs104894650
1000 genomes	rs104894650
hgdp	rs104894650
ensembl	rs104894650
geneview	rs104894650
scholar	rs104894650
google	rs104894650
pharmgkb	rs104894650
gwascentral	rs104894650
openSNP	rs104894650
23andMe	rs104894650
SNPshot	rs104894650
SNPdbe	rs104894650
MSV3d	rs104894650
GWAS Ctlg	rs104894650

Max Magnitude

0

OMIM	604907
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894650(A;A) rs104894650(G;G) rs104894650(T;T)
Alt	rs104894650(A;A) rs104894650(G;G) rs104894650(T;T)
Reference	Rs104894650(C;C)
Significance	Pathogenic
Disease	not provided Common variable immunodeficiency 2
Variation	info
Gene	TNFRSF13B
CLNDBN	not provided Common variable immunodeficiency 2
Reversed	1
HGVS	NC_000017.10:g.16852066G>C; NC_000017.10:g.16852066G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000255478.2, RCV000005631.2,