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rs63750585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750585(G;G)
Make rs63750585(G;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position172920
GeneHBA2
is asnp
is mentioned by
dbSNPrs63750585
ebirs63750585
HLIrs63750585
Exacrs63750585
Varsomers63750585
Maprs63750585
PheGenIrs63750585
hapmaprs63750585
1000 genomesrs63750585
hgdprs63750585
ensemblrs63750585
gopubmedrs63750585
geneviewrs63750585
scholarrs63750585
googlers63750585
pharmgkbrs63750585
gwascentralrs63750585
openSNPrs63750585
23andMers63750585
23andMe allrs63750585
SNP Nexus

SNPshotrs63750585
SNPdbers63750585
MSV3drs63750585
GWAS Ctlgrs63750585
Max Magnitude0
OMIM141800
Desc
Variant0021
Relatedalso


ClinVar
Risk rs63750585(C,G;C,G)
Alt rs63750585(C,G;C,G)
Reference rs63750585(T;T)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.222919T>C; NC_000016.9:g.222919T>G
CLNSRC
CLNACC



[PMID 6526652] Hemoglobin Chongqing [alpha 2(NA2)Leu----Arg] and hemoglobin Harbin [alpha 16(A14)Lys----Met] found in China.