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rs33939421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33939421(A;T)
Make rs33939421(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position176787
GeneHBA1
is asnp
is mentioned by
dbSNPrs33939421
dbSNP (classic)rs33939421
ClinGenrs33939421
ebirs33939421
HLIrs33939421
Exacrs33939421
Gnomadrs33939421
Varsomers33939421
LitVarrs33939421
Maprs33939421
PheGenIrs33939421
Biobankrs33939421
1000 genomesrs33939421
hgdprs33939421
ensemblrs33939421
geneviewrs33939421
scholarrs33939421
googlers33939421
pharmgkbrs33939421
gwascentralrs33939421
openSNPrs33939421
23andMers33939421
SNPshotrs33939421
SNPdbers33939421
MSV3drs33939421
GWAS Ctlgrs33939421
Max Magnitude0
OMIM141800
Desc
Variant0035
Relatedalso
OMIM141800
Desc
Variant0124
Relatedalso
ClinVar
Risk rs33939421(G;G) rs33939421(T;T)
Alt rs33939421(G;G) rs33939421(T;T)
Reference Rs33939421(A;A)
Significance Other
Disease HEMOGLOBIN REIMS HEMOGLOBIN G (AUDHALI)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN REIMS HEMOGLOBIN G (AUDHALI)
Reversed 0
HGVS NC_000016.9:g.226786A>G; NC_000016.9:g.226786A>T
CLNSRC HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017146.2, RCV000017022.2,


[PMID 5675637] Plasma spermine oxidase in relation to fermentation in hippopotamus stomach.


[PMID 2634669] Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability.