rs1057519074

Orientation

plus

Stabilized

plus

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

Make rs1057519074(C;T)

Make rs1057519074(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

65731150

Gene

MSN

is a	snp
is	mentioned by
dbSNP	rs1057519074
dbSNP (classic)	rs1057519074
ClinGen	rs1057519074
ebi	rs1057519074
HLI	rs1057519074
Exac	rs1057519074
Gnomad	rs1057519074
Varsome	rs1057519074
LitVar	rs1057519074
Map	rs1057519074
PheGenI	rs1057519074
Biobank	rs1057519074
1000 genomes	rs1057519074
hgdp	rs1057519074
ensembl	rs1057519074
geneview	rs1057519074
scholar	rs1057519074
google	rs1057519074
pharmgkb	rs1057519074
gwascentral	rs1057519074
openSNP	rs1057519074
23andMe	rs1057519074
SNPshot	rs1057519074
SNPdbe	rs1057519074
MSV3d	rs1057519074
GWAS Ctlg	rs1057519074

Max Magnitude

0

ClinVar
Risk	rs1057519074(T;T)
Alt	rs1057519074(T;T)
Reference	Rs1057519074(C;C)
Significance	Pathogenic
Disease	Immunodeficiency 50
Variation	info
Gene	MSN
CLNDBN	Immunodeficiency 50
Reversed	0
HGVS	NC_000023.10:g.64951012C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412603.1,