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rs63750679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750679(A;A)
Make rs63750679(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position172968
GeneHBA2
is asnp
is mentioned by
dbSNPrs63750679
ebirs63750679
HLIrs63750679
Exacrs63750679
Varsomers63750679
Maprs63750679
PheGenIrs63750679
hapmaprs63750679
1000 genomesrs63750679
hgdprs63750679
ensemblrs63750679
gopubmedrs63750679
geneviewrs63750679
scholarrs63750679
googlers63750679
pharmgkbrs63750679
gwascentralrs63750679
openSNPrs63750679
23andMers63750679
23andMe allrs63750679
SNP Nexus

SNPshotrs63750679
SNPdbers63750679
MSV3drs63750679
GWAS Ctlgrs63750679
Max Magnitude0
OMIM141800
Desc
Variant0175
Relatedalso
ClinVar
Risk rs63750679(A;A)
Alt rs63750679(A;A)
Reference rs63750679(G;G)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.222967G>A
CLNSRC
CLNACC


[PMID 1428941] HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family.