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rs35859529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35859529(A;G)
Make rs35859529(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177051
GeneHBA1
is asnp
is mentioned by
dbSNPrs35859529
ebirs35859529
HLIrs35859529
Exacrs35859529
Varsomers35859529
Maprs35859529
PheGenIrs35859529
hapmaprs35859529
1000 genomesrs35859529
hgdprs35859529
ensemblrs35859529
gopubmedrs35859529
geneviewrs35859529
scholarrs35859529
googlers35859529
pharmgkbrs35859529
gwascentralrs35859529
openSNPrs35859529
23andMers35859529
23andMe allrs35859529
SNP Nexus

SNPshotrs35859529
SNPdbers35859529
MSV3drs35859529
GWAS Ctlgrs35859529
Max Magnitude0
OMIM141800
Desc
Variant0026
Relatedalso
ClinVar
Risk rs35859529(G;G)
Alt rs35859529(G;G)
Reference rs35859529(A;A)
Significance Other
Disease HEMOGLOBIN DANESHGAH-TEHRAN
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN DANESHGAH-TEHRAN
Reversed 0
HGVS NC_000016.9:g.227050A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017013.2,


[PMID 3841101] Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family.


[PMID 4518991] Haemoglobin Daneshgah-Tehran alpha2 72 (EPI) histidine--arginine betaA2.