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rs35187567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35187567(A;A)
Make rs35187567(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position173535
GeneHBA2
is asnp
is mentioned by
dbSNPrs35187567
ebirs35187567
HLIrs35187567
Exacrs35187567
Varsomers35187567
Maprs35187567
PheGenIrs35187567
hapmaprs35187567
1000 genomesrs35187567
hgdprs35187567
ensemblrs35187567
gopubmedrs35187567
geneviewrs35187567
scholarrs35187567
googlers35187567
pharmgkbrs35187567
gwascentralrs35187567
openSNPrs35187567
23andMers35187567
23andMe allrs35187567
SNP Nexus

SNPshotrs35187567
SNPdbers35187567
MSV3drs35187567
GWAS Ctlgrs35187567
Max Magnitude0
OMIM141800
Desc
Variant0115
Relatedalso
ClinVar
Risk rs35187567(A;A)
Alt rs35187567(A;A)
Reference rs35187567(G;G)
Significance Untested
Disease
Variation info
Gene HBA2
CLNDBN
Reversed 0
HGVS NC_000016.9:g.223534G>A
CLNSRC
CLNACC



[PMID 3754245] Hb Owari [alpha 121 (H 4) Val----Met]: a new hemoglobin variant with a neutral-to-neutral amino acid substitution detected by isoelectric focusing.