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rs35239527

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35239527(G;T)
Make rs35239527(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177098
GeneHBA1
is asnp
is mentioned by
dbSNPrs35239527
ebirs35239527
HLIrs35239527
Exacrs35239527
Varsomers35239527
Maprs35239527
PheGenIrs35239527
hapmaprs35239527
1000 genomesrs35239527
hgdprs35239527
ensemblrs35239527
gopubmedrs35239527
geneviewrs35239527
scholarrs35239527
googlers35239527
pharmgkbrs35239527
gwascentralrs35239527
openSNPrs35239527
23andMers35239527
23andMe allrs35239527
SNP Nexus

SNPshotrs35239527
SNPdbers35239527
MSV3drs35239527
GWAS Ctlgrs35239527
Max Magnitude0
OMIM141800
Desc
Variant0090
Relatedalso
ClinVar
Risk rs35239527(T;T)
Alt rs35239527(T;T)
Reference rs35239527(G;G)
Significance Other
Disease HEMOGLOBIN LOIRE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN LOIRE
Reversed 0
HGVS NC_000016.9:g.227097G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017096.2,


[PMID 3142772] Increased oxygen affinity with normal heterotropic effects in hemoglobin Loire [alpha 88(F9)Ala----Ser].