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rs1057519637

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1057519637(-;-)
Make rs1057519637(-;AG)
Make rs1057519637(AG;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position173006
GeneHBA2
is asnp
is mentioned by
dbSNPrs1057519637
dbSNP (old)rs1057519637
ClinGenrs1057519637
ebirs1057519637
HLIrs1057519637
Exacrs1057519637
Gnomadrs1057519637
Varsomers1057519637
Maprs1057519637
PheGenIrs1057519637
Biobankrs1057519637
1000 genomesrs1057519637
hgdprs1057519637
ensemblrs1057519637
gopubmedrs1057519637
geneviewrs1057519637
scholarrs1057519637
googlers1057519637
pharmgkbrs1057519637
gwascentralrs1057519637
openSNPrs1057519637
23andMers1057519637
23andMe allrs1057519637
SNPshotrs1057519637
SNPdbers1057519637
MSV3drs1057519637
GWAS Ctlgrs1057519637
Max Magnitude0
ClinVar
Risk rs1057519637(-;-)
Alt rs1057519637(-;-)
Reference Rs1057519637(GA;GA)
Significance Pathogenic
Disease Alpha Thalassemia
Variation info
Gene HBA2
CLNDBN alpha Thalassemia
Reversed 0
HGVS NC_000016.9:g.223005_223006delAG
CLNSRC
CLNACC RCV000417216.1,