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rs35746147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35746147(A;A)
Make rs35746147(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249522
GeneHBG1
is asnp
is mentioned by
dbSNPrs35746147
ebirs35746147
HLIrs35746147
Exacrs35746147
Varsomers35746147
Maprs35746147
PheGenIrs35746147
hapmaprs35746147
1000 genomesrs35746147
hgdprs35746147
ensemblrs35746147
gopubmedrs35746147
geneviewrs35746147
scholarrs35746147
googlers35746147
pharmgkbrs35746147
gwascentralrs35746147
openSNPrs35746147
23andMers35746147
23andMe allrs35746147
SNP Nexus

SNPshotrs35746147
SNPdbers35746147
MSV3drs35746147
GWAS Ctlgrs35746147
Max Magnitude0
OMIM142200
Desc
Variant0003
Relatedalso


ClinVar
Risk rs35746147(A;A)
Alt rs35746147(A;A)
Reference rs35746147(C;C)
Significance Other
Disease HEMOGLOBIN F (BEECH ISLAND)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (BEECH ISLAND)
Reversed 1
HGVS NC_000011.9:g.5270752G>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016147.1,



[PMID 2417989] Hb F-Beech Island or alpha 2A gamma 2(53)(D4)Ala----Asp.