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rs63749934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs63749934(C;C)
Make rs63749934(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position173196
GeneHBA2
is asnp
is mentioned by
dbSNPrs63749934
ebirs63749934
HLIrs63749934
Exacrs63749934
Varsomers63749934
Maprs63749934
PheGenIrs63749934
hapmaprs63749934
1000 genomesrs63749934
hgdprs63749934
ensemblrs63749934
gopubmedrs63749934
geneviewrs63749934
scholarrs63749934
googlers63749934
pharmgkbrs63749934
gwascentralrs63749934
openSNPrs63749934
23andMers63749934
23andMe allrs63749934
SNP Nexus

SNPshotrs63749934
SNPdbers63749934
MSV3drs63749934
GWAS Ctlgrs63749934
Max Magnitude0
OMIM141850
Desc
Variant0046
Relatedalso


ClinVar
Risk rs63749934(C;C)
Alt rs63749934(C;C)
Reference rs63749934(T;T)
Significance Other
Disease HEMOGLOBIN GERLAND
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN GERLAND
Reversed 0
HGVS NC_000016.9:g.223195T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016956.1,



[PMID 11791875] Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.