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

rs34460332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34460332(A;A)
Make rs34460332(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5234360
GeneHBD
is asnp
is mentioned by
dbSNPrs34460332
ebirs34460332
HLIrs34460332
Exacrs34460332
Varsomers34460332
Maprs34460332
PheGenIrs34460332
hapmaprs34460332
1000 genomesrs34460332
hgdprs34460332
ensemblrs34460332
gopubmedrs34460332
geneviewrs34460332
scholarrs34460332
googlers34460332
pharmgkbrs34460332
gwascentralrs34460332
openSNPrs34460332
23andMers34460332
23andMe allrs34460332
SNP Nexus

SNPshotrs34460332
SNPdbers34460332
MSV3drs34460332
GWAS Ctlgrs34460332
Max Magnitude0
OMIM142000
Desc
Variant0015
Relatedalso
? (A;G) (G;G)
ClinVar
Risk rs34460332(A;A)
Alt rs34460332(A;A)
Reference rs34460332(G;G)
Significance Other
Disease HEMOGLOBIN A(2) VICTORIA
Variation info
Gene HBD
CLNDBN HEMOGLOBIN A(2) VICTORIA
Reversed 1
HGVS NC_000011.9:g.5255590C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016203.1,



[PMID 6469695] HbA2 Victoria delta 24 (B6) Gly----Asp. A new delta chain variant occurring with beta-thalassemia.