rs104894764

Orientation

plus

Stabilized

plus

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

Make rs104894764(G;T)

Make rs104894764(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

123886014

Gene

XIAP

is a	snp
is	mentioned by
dbSNP	rs104894764
dbSNP (classic)	rs104894764
ClinGen	rs104894764
ebi	rs104894764
HLI	rs104894764
Exac	rs104894764
Gnomad	rs104894764
Varsome	rs104894764
LitVar	rs104894764
Map	rs104894764
PheGenI	rs104894764
Biobank	rs104894764
1000 genomes	rs104894764
hgdp	rs104894764
ensembl	rs104894764
geneview	rs104894764
scholar	rs104894764
google	rs104894764
pharmgkb	rs104894764
gwascentral	rs104894764
openSNP	rs104894764
23andMe	rs104894764
SNPshot	rs104894764
SNPdbe	rs104894764
MSV3d	rs104894764
GWAS Ctlg	rs104894764

Max Magnitude

0

OMIM	300079
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894764(T;T)
Alt	rs104894764(T;T)
Reference	Rs104894764(G;G)
Significance	Pathogenic
Disease	Lymphoproliferative syndrome 2
Variation	info
Gene	XIAP
CLNDBN	Lymphoproliferative syndrome 2, X-linked
Reversed	0
HGVS	NC_000023.10:g.123019864G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012412.23,