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rs111033628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033628(C;T)
Make rs111033628(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position124365795
GeneSH2D1A
is asnp
is mentioned by
dbSNPrs111033628
ebirs111033628
HLIrs111033628
Exacrs111033628
Varsomers111033628
Maprs111033628
PheGenIrs111033628
hapmaprs111033628
1000 genomesrs111033628
hgdprs111033628
ensemblrs111033628
gopubmedrs111033628
geneviewrs111033628
scholarrs111033628
googlers111033628
pharmgkbrs111033628
gwascentralrs111033628
openSNPrs111033628
23andMers111033628
23andMe allrs111033628
SNP Nexus

SNPshotrs111033628
SNPdbers111033628
MSV3drs111033628
GWAS Ctlgrs111033628
Max Magnitude0
OMIM300490
Desc
Variant0002
Relatedalso
ClinVar
Risk rs111033628(T;T)
Alt rs111033628(T;T)
Reference rs111033628(C;C)
Significance Pathogenic
Disease Lymphoproliferative syndrome 1
Variation info
Gene SH2D1A
CLNDBN Lymphoproliferative syndrome 1, X-linked
Reversed 0
HGVS NC_000023.10:g.123499645C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011646.9,