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rs1060339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060339(A;A)
Make rs1060339(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position177040
GeneHBA1
is asnp
is mentioned by
dbSNPrs1060339
dbSNP (classic)rs1060339
ClinGenrs1060339
ebirs1060339
HLIrs1060339
Exacrs1060339
Gnomadrs1060339
Varsomers1060339
LitVarrs1060339
Maprs1060339
PheGenIrs1060339
Biobankrs1060339
1000 genomesrs1060339
hgdprs1060339
ensemblrs1060339
geneviewrs1060339
scholarrs1060339
googlers1060339
pharmgkbrs1060339
gwascentralrs1060339
openSNPrs1060339
23andMers1060339
23andMe allrs1060339
SNPshotrs1060339
SNPdbers1060339
MSV3drs1060339
GWAS Ctlgrs1060339
Max Magnitude0
ClinVar
Risk rs1060339(A;A) rs1060339(G;G)
Alt rs1060339(A;A) rs1060339(G;G)
Reference Rs1060339(C;C)
Significance Pathogenic
Disease Alpha Thalassemia
Variation info
Gene HBA1
CLNDBN alpha Thalassemia
Reversed 0
HGVS NC_000016.9:g.227039C>A
CLNSRC
CLNACC RCV000417227.1,