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rs1057519075

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519075(C;T)
Make rs1057519075(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position65739816
GeneMSN
is asnp
is mentioned by
dbSNPrs1057519075
dbSNP (old)rs1057519075
ClinGenrs1057519075
ebirs1057519075
HLIrs1057519075
Exacrs1057519075
Gnomadrs1057519075
Varsomers1057519075
Maprs1057519075
PheGenIrs1057519075
Biobankrs1057519075
1000 genomesrs1057519075
hgdprs1057519075
ensemblrs1057519075
gopubmedrs1057519075
geneviewrs1057519075
scholarrs1057519075
googlers1057519075
pharmgkbrs1057519075
gwascentralrs1057519075
openSNPrs1057519075
23andMers1057519075
23andMe allrs1057519075
SNPshotrs1057519075
SNPdbers1057519075
MSV3drs1057519075
GWAS Ctlgrs1057519075
Max Magnitude0
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,