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rs111033625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033625(A;A)
Make rs111033625(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position124371389
GeneSH2D1A
is asnp
is mentioned by
dbSNPrs111033625
ebirs111033625
HLIrs111033625
Exacrs111033625
Varsomers111033625
Maprs111033625
PheGenIrs111033625
hapmaprs111033625
1000 genomesrs111033625
hgdprs111033625
ensemblrs111033625
gopubmedrs111033625
geneviewrs111033625
scholarrs111033625
googlers111033625
pharmgkbrs111033625
gwascentralrs111033625
openSNPrs111033625
23andMers111033625
23andMe allrs111033625
SNP Nexus

SNPshotrs111033625
SNPdbers111033625
MSV3drs111033625
GWAS Ctlgrs111033625
Max Magnitude0
OMIM300490
Desc
Variant0006
Relatedalso
ClinVar
Risk rs111033625(A;A)
Alt rs111033625(A;A)
Reference rs111033625(T;T)
Significance Pathogenic
Disease Lymphoproliferative syndrome 1
Variation info
Gene SH2D1A
CLNDBN Lymphoproliferative syndrome 1, X-linked
Reversed 0
HGVS NC_000023.10:g.123505239T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011650.6,