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rs36075744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs36075744(A;A)
Make rs36075744(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173533
GeneHBA2
is asnp
is mentioned by
dbSNPrs36075744
ebirs36075744
HLIrs36075744
Exacrs36075744
Varsomers36075744
Maprs36075744
PheGenIrs36075744
hapmaprs36075744
1000 genomesrs36075744
hgdprs36075744
ensemblrs36075744
gopubmedrs36075744
geneviewrs36075744
scholarrs36075744
googlers36075744
pharmgkbrs36075744
gwascentralrs36075744
openSNPrs36075744
23andMers36075744
23andMe allrs36075744
SNP Nexus

SNPshotrs36075744
SNPdbers36075744
MSV3drs36075744
GWAS Ctlgrs36075744
Max Magnitude0
OMIM141800
Desc
Variant0060
Relatedalso
ClinVar
Risk rs36075744(A;A)
Alt rs36075744(A;A)
Reference rs36075744(C;C)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223532C>A
CLNSRC
CLNACC



[PMID 2737912] Hb J-Meerut [alpha 120(H3)Ala----Glu] found in a Japanese family.


[PMID 4600474] Hemoglobin J Meerut: alpha120 Ala leads to Glu.


[PMID 7713747] A case of HB J-Meerut (or Hb J-Birmingham) [alpha 120(H3)Ala-->Glu].


[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.