rs104894776

Orientation

plus

Stabilized

plus

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

Make rs104894776(A;A)

Make rs104894776(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

136659049

Gene

CD40LG

is a	snp
is	mentioned by
dbSNP	rs104894776
dbSNP (classic)	rs104894776
ClinGen	rs104894776
ebi	rs104894776
HLI	rs104894776
Exac	rs104894776
Gnomad	rs104894776
Varsome	rs104894776
LitVar	rs104894776
Map	rs104894776
PheGenI	rs104894776
Biobank	rs104894776
1000 genomes	rs104894776
hgdp	rs104894776
ensembl	rs104894776
geneview	rs104894776
scholar	rs104894776
google	rs104894776
pharmgkb	rs104894776
gwascentral	rs104894776
openSNP	rs104894776
23andMe	rs104894776
SNPshot	rs104894776
SNPdbe	rs104894776
MSV3d	rs104894776
GWAS Ctlg	rs104894776

Max Magnitude

0

OMIM	300386
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104894776(A;A)
Alt	rs104894776(A;A)
Reference	Rs104894776(G;G)
Significance	Untested
Disease	Immunodeficiency with hyper IgM type 1
Variation	info
Gene	CD40LG
CLNDBN	Immunodeficiency with hyper IgM type 1
Reversed	0
HGVS	NC_000023.10:g.135741208G>A
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000032146.1, SCV000032146.1,