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rs387906631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common genotype
Make rs387906631(C;T)
Make rs387906631(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome3
Position128481901
GeneGATA2
is asnp
is mentioned by
dbSNPrs387906631
dbSNP (classic)rs387906631
ClinGenrs387906631
ebirs387906631
HLIrs387906631
Exacrs387906631
Gnomadrs387906631
Varsomers387906631
LitVarrs387906631
Maprs387906631
PheGenIrs387906631
Biobankrs387906631
1000 genomesrs387906631
hgdprs387906631
ensemblrs387906631
geneviewrs387906631
scholarrs387906631
googlers387906631
pharmgkbrs387906631
gwascentralrs387906631
openSNPrs387906631
23andMers387906631
SNPshotrs387906631
SNPdbers387906631
MSV3drs387906631
GWAS Ctlgrs387906631
Max Magnitude0

aka NM_001145661.1(GATA2):c.1061C>T or (p.Thr354Met)

OMIM pathogenic variant