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rs41338947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41338947(A;A)
Make rs41338947(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173323
GeneHBA2
is asnp
is mentioned by
dbSNPrs41338947
ebirs41338947
HLIrs41338947
Exacrs41338947
Varsomers41338947
Maprs41338947
PheGenIrs41338947
hapmaprs41338947
1000 genomesrs41338947
hgdprs41338947
ensemblrs41338947
gopubmedrs41338947
geneviewrs41338947
scholarrs41338947
googlers41338947
pharmgkbrs41338947
gwascentralrs41338947
openSNPrs41338947
23andMers41338947
23andMe allrs41338947
SNP Nexus

SNPshotrs41338947
SNPdbers41338947
MSV3drs41338947
GWAS Ctlgrs41338947
Max Magnitude0
OMIM141800
Desc
Variant0025
Relatedalso
ClinVar
Risk rs41338947(A;A)
Alt rs41338947(A;A)
Reference rs41338947(C;C)
Significance Other
Disease HEMOGLOBIN DALLAS
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN DALLAS
Reversed 0
HGVS NC_000016.9:g.223322C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017012.1,



[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.