rs1057519075

Orientation

plus

Stabilized

plus

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

Make rs1057519075(C;T)

Make rs1057519075(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

65739816

Gene

MSN

is a	snp
is	mentioned by
dbSNP	rs1057519075
dbSNP (classic)	rs1057519075
ClinGen	rs1057519075
ebi	rs1057519075
HLI	rs1057519075
Exac	rs1057519075
Gnomad	rs1057519075
Varsome	rs1057519075
LitVar	rs1057519075
Map	rs1057519075
PheGenI	rs1057519075
Biobank	rs1057519075
1000 genomes	rs1057519075
hgdp	rs1057519075
ensembl	rs1057519075
geneview	rs1057519075
scholar	rs1057519075
google	rs1057519075
pharmgkb	rs1057519075
gwascentral	rs1057519075
openSNP	rs1057519075
23andMe	rs1057519075
SNPshot	rs1057519075
SNPdbe	rs1057519075
MSV3d	rs1057519075
GWAS Ctlg	rs1057519075

Max Magnitude

0

ClinVar
Risk	rs1057519075(T;T)
Alt	rs1057519075(T;T)
Reference	Rs1057519075(C;C)
Significance	Pathogenic
Disease	Immunodeficiency 50
Variation	info
Gene	MSN
CLNDBN	Immunodeficiency 50
Reversed	0
HGVS	NC_000023.10:g.64959678C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412497.1,