Have questions? Visit https://www.reddit.com/r/SNPedia

rs34282684

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs34282684(-;-)
Make rs34282684(-;GT)
Make rs34282684(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position5226689
GeneHBB
is asnp
is mentioned by
dbSNPrs34282684
ebirs34282684
HLIrs34282684
Exacrs34282684
Varsomers34282684
Maprs34282684
PheGenIrs34282684
hapmaprs34282684
1000 genomesrs34282684
hgdprs34282684
ensemblrs34282684
gopubmedrs34282684
geneviewrs34282684
scholarrs34282684
googlers34282684
pharmgkbrs34282684
gwascentralrs34282684
openSNPrs34282684
23andMers34282684
23andMe allrs34282684
SNP Nexus

SNPshotrs34282684
SNPdbers34282684
MSV3drs34282684
GWAS Ctlgrs34282684
Max Magnitude0
ClinVar
Risk rs34282684(;)
Alt rs34282684(;)
Reference rs34282684(TG;TG)
Significance Probable-Pathogenic
Disease Beta thalassemia major
Variation info
Gene HBB
CLNDBN Beta thalassemia major
Reversed 1
HGVS NC_000011.9:g.5247918_5247919delCA
CLNSRC
CLNACC RCV000029968.1,