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rs35776155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35776155(C;T)
Make rs35776155(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position176946
GeneHBA1
is asnp
is mentioned by
dbSNPrs35776155
ebirs35776155
HLIrs35776155
Exacrs35776155
Varsomers35776155
Maprs35776155
PheGenIrs35776155
hapmaprs35776155
1000 genomesrs35776155
hgdprs35776155
ensemblrs35776155
gopubmedrs35776155
geneviewrs35776155
scholarrs35776155
googlers35776155
pharmgkbrs35776155
gwascentralrs35776155
openSNPrs35776155
23andMers35776155
23andMe allrs35776155
SNP Nexus

SNPshotrs35776155
SNPdbers35776155
MSV3drs35776155
GWAS Ctlgrs35776155
Max Magnitude0
OMIM141800
Desc
Variant0012
Relatedalso
OMIM141850
Desc
Variant0053
Relatedalso
ClinVar
Risk rs35776155(G,T;G,T)
Alt rs35776155(G,T;G,T)
Reference rs35776155(C;C)
Significance Other
Disease HEMOGLOBIN BOURMEDES
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN BOURMEDES
Reversed 0
HGVS NC_000016.9:g.226945C>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016998.2,


[PMID 3438164] [Hemoglobin Boumerdes alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].