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rs1057519074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519074(C;T)
Make rs1057519074(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position65731150
GeneMSN
is asnp
is mentioned by
dbSNPrs1057519074
dbSNP (classic)rs1057519074
ClinGenrs1057519074
ebirs1057519074
HLIrs1057519074
Exacrs1057519074
Gnomadrs1057519074
Varsomers1057519074
LitVarrs1057519074
Maprs1057519074
PheGenIrs1057519074
Biobankrs1057519074
1000 genomesrs1057519074
hgdprs1057519074
ensemblrs1057519074
geneviewrs1057519074
scholarrs1057519074
googlers1057519074
pharmgkbrs1057519074
gwascentralrs1057519074
openSNPrs1057519074
23andMers1057519074
23andMe allrs1057519074
SNPshotrs1057519074
SNPdbers1057519074
MSV3drs1057519074
GWAS Ctlgrs1057519074
Max Magnitude0
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,