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rs35993097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35993097(A;A)
Make rs35993097(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176772
GeneHBA1
is asnp
is mentioned by
dbSNPrs35993097
ebirs35993097
HLIrs35993097
Exacrs35993097
Varsomers35993097
Maprs35993097
PheGenIrs35993097
hapmaprs35993097
1000 genomesrs35993097
hgdprs35993097
ensemblrs35993097
gopubmedrs35993097
geneviewrs35993097
scholarrs35993097
googlers35993097
pharmgkbrs35993097
gwascentralrs35993097
openSNPrs35993097
23andMers35993097
23andMe allrs35993097
SNP Nexus

SNPshotrs35993097
SNPdbers35993097
MSV3drs35993097
GWAS Ctlgrs35993097
Max Magnitude0
OMIM141800
Desc
Variant0175
Relatedalso
ClinVar
Risk rs35993097(A;A)
Alt rs35993097(A;A)
Reference rs35993097(G;G)
Significance Other
Disease HEMOGLOBIN AL-AIN ABU DHABI
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN AL-AIN ABU DHABI
Reversed 0
HGVS NC_000016.9:g.226771G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017195.2,


[PMID 1428941] HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family.