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rs104894163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894163(A;A)
Make rs104894163(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position8064037
GeneGATA3
is asnp
is mentioned by
dbSNPrs104894163
dbSNP (classic)rs104894163
ClinGenrs104894163
ebirs104894163
HLIrs104894163
Exacrs104894163
Gnomadrs104894163
Varsomers104894163
LitVarrs104894163
Maprs104894163
PheGenIrs104894163
Biobankrs104894163
1000 genomesrs104894163
hgdprs104894163
ensemblrs104894163
geneviewrs104894163
scholarrs104894163
googlers104894163
pharmgkbrs104894163
gwascentralrs104894163
openSNPrs104894163
23andMers104894163
SNPshotrs104894163
SNPdbers104894163
MSV3drs104894163
GWAS Ctlgrs104894163
Max Magnitude0
OMIM131320
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894163(A;A)
Alt rs104894163(A;A)
Reference Rs104894163(T;T)
Significance Pathogenic
Disease Barakat syndrome
Variation info
Gene GATA3
CLNDBN Barakat syndrome
Reversed 0
HGVS NC_000010.10:g.8106000T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018103.28,