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rs35960772

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35960772(A;G)
Make rs35960772(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226639
GeneHBB
is asnp
is mentioned by
dbSNPrs35960772
ebirs35960772
HLIrs35960772
Exacrs35960772
Varsomers35960772
Maprs35960772
PheGenIrs35960772
hapmaprs35960772
1000 genomesrs35960772
hgdprs35960772
ensemblrs35960772
gopubmedrs35960772
geneviewrs35960772
scholarrs35960772
googlers35960772
pharmgkbrs35960772
gwascentralrs35960772
openSNPrs35960772
23andMers35960772
23andMe allrs35960772
SNP Nexus

SNPshotrs35960772
SNPdbers35960772
MSV3drs35960772
GWAS Ctlgrs35960772
Max Magnitude0
OMIM141900
Desc
Variant0491
Relatedalso


ClinVar
Risk rs35960772(G;G)
Alt rs35960772(G;G)
Reference rs35960772(A;A)
Significance Other
Disease HEMOGLOBIN SAALE
Variation info
Gene HBB
CLNDBN HEMOGLOBIN SAALE
Reversed 1
HGVS NC_000011.9:g.5247869T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016846.2,



[PMID 10770934] Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.