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rs111033598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033598(C;C)
Make rs111033598(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position173212
GeneHBA2
is asnp
is mentioned by
dbSNPrs111033598
ebirs111033598
HLIrs111033598
Exacrs111033598
Varsomers111033598
Maprs111033598
PheGenIrs111033598
hapmaprs111033598
1000 genomesrs111033598
hgdprs111033598
ensemblrs111033598
gopubmedrs111033598
geneviewrs111033598
scholarrs111033598
googlers111033598
pharmgkbrs111033598
gwascentralrs111033598
openSNPrs111033598
23andMers111033598
23andMe allrs111033598
SNP Nexus

SNPshotrs111033598
SNPdbers111033598
MSV3drs111033598
GWAS Ctlgrs111033598
Max Magnitude0
OMIM141850
Desc
Variant0008
Relatedalso
ClinVar
Risk rs111033598(C,T;C,T)
Alt rs111033598(C,T;C,T)
Reference rs111033598(G;G)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223211G>C; NC_000016.9:g.223211G>T
CLNSRC
CLNACC


[PMID 5356548OA-icon.png] Abnormal haemoglobins in Zambia. A new haemoglobin Zambia alpha-60 (E9) lysine--asparagine.