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rs33957766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33957766(A;T)
Make rs33957766(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position173551
GeneHBA2
is asnp
is mentioned by
dbSNPrs33957766
ebirs33957766
HLIrs33957766
Exacrs33957766
Varsomers33957766
Maprs33957766
PheGenIrs33957766
hapmaprs33957766
1000 genomesrs33957766
hgdprs33957766
ensemblrs33957766
gopubmedrs33957766
geneviewrs33957766
scholarrs33957766
googlers33957766
pharmgkbrs33957766
gwascentralrs33957766
openSNPrs33957766
23andMers33957766
23andMe allrs33957766
SNP Nexus

SNPshotrs33957766
SNPdbers33957766
MSV3drs33957766
GWAS Ctlgrs33957766
Max Magnitude0
OMIM141800
Desc
Variant0163
Relatedalso
ClinVar
Risk rs33957766(G,T;G,T)
Alt rs33957766(G,T;G,T)
Reference rs33957766(A;A)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223550A>G; NC_000016.9:g.223550A>T
CLNSRC
CLNACC


[PMID 2079432] Hb Fukutomi [alpha 126(H9)Asp----Val]: a new hemoglobin variant with high oxygen affinity.