Have questions? Visit https://www.reddit.com/r/SNPedia

rs63749809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs63749809(A;A)
Make rs63749809(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position173578
GeneHBA2
is asnp
is mentioned by
dbSNPrs63749809
ebirs63749809
HLIrs63749809
Exacrs63749809
Varsomers63749809
Maprs63749809
PheGenIrs63749809
hapmaprs63749809
1000 genomesrs63749809
hgdprs63749809
ensemblrs63749809
gopubmedrs63749809
geneviewrs63749809
scholarrs63749809
googlers63749809
pharmgkbrs63749809
gwascentralrs63749809
openSNPrs63749809
23andMers63749809
23andMe allrs63749809
SNP Nexus

SNPshotrs63749809
SNPdbers63749809
MSV3drs63749809
GWAS Ctlgrs63749809
Max Magnitude0
OMIM141800
Desc
Variant0166
Relatedalso


ClinVar
Risk rs63749809(A;A)
Alt rs63749809(A;A)
Reference rs63749809(T;T)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223577T>A
CLNSRC
CLNACC



[PMID 2347082] A new hemoglobin variant found during investigations of diabetes mellitus: Hb Pavie [alpha 135 (H18) Val----Glu].