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rs41364652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41364652(A;A)
Make rs41364652(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173580
GeneHBA2
is asnp
is mentioned by
dbSNPrs41364652
ebirs41364652
HLIrs41364652
Exacrs41364652
Varsomers41364652
Maprs41364652
PheGenIrs41364652
hapmaprs41364652
1000 genomesrs41364652
hgdprs41364652
ensemblrs41364652
gopubmedrs41364652
geneviewrs41364652
scholarrs41364652
googlers41364652
pharmgkbrs41364652
gwascentralrs41364652
openSNPrs41364652
23andMers41364652
23andMe allrs41364652
SNP Nexus

SNPshotrs41364652
SNPdbers41364652
MSV3drs41364652
GWAS Ctlgrs41364652
Max Magnitude0
OMIM141800
Desc
Variant0020
Relatedalso


ClinVar
Risk rs41364652(A;A)
Alt rs41364652(A;A)
Reference rs41364652(C;C)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223579C>A
CLNSRC
CLNACC



[PMID 3781866] HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black family.


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


[PMID 8226092] Three sickle cell anemia patients each with a different alpha chain variant. Diagnostic complications.