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rs104894815

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894815(A;A)
Make rs104894815(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position48792337
GeneGATA1
is asnp
is mentioned by
dbSNPrs104894815
dbSNP (classic)rs104894815
ClinGenrs104894815
ebirs104894815
HLIrs104894815
Exacrs104894815
Gnomadrs104894815
Varsomers104894815
LitVarrs104894815
Maprs104894815
PheGenIrs104894815
Biobankrs104894815
1000 genomesrs104894815
hgdprs104894815
ensemblrs104894815
geneviewrs104894815
scholarrs104894815
googlers104894815
pharmgkbrs104894815
gwascentralrs104894815
openSNPrs104894815
23andMers104894815
SNPshotrs104894815
SNPdbers104894815
MSV3drs104894815
GWAS Ctlgrs104894815
Max Magnitude0
OMIM305371
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894815(A;A)
Alt rs104894815(A;A)
Reference Rs104894815(G;G)
Significance Pathogenic
Disease Dyserythropoietic anemia with thrombocytopenia GATA-1-related thrombocytopenia with dyserythropoiesis
Variation info
Gene GATA1
CLNDBN Dyserythropoietic anemia with thrombocytopenia GATA-1-related thrombocytopenia with dyserythropoiesis
Reversed 0
HGVS NC_000023.10:g.48650744G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000011168.5, RCV000144255.2,