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rs35977759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35977759(A;G)
Make rs35977759(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249564
GeneHBG1
is asnp
is mentioned by
dbSNPrs35977759
ebirs35977759
HLIrs35977759
Exacrs35977759
Varsomers35977759
Maprs35977759
PheGenIrs35977759
hapmaprs35977759
1000 genomesrs35977759
hgdprs35977759
ensemblrs35977759
gopubmedrs35977759
geneviewrs35977759
scholarrs35977759
googlers35977759
pharmgkbrs35977759
gwascentralrs35977759
openSNPrs35977759
23andMers35977759
23andMe allrs35977759
SNP Nexus

SNPshotrs35977759
SNPdbers35977759
MSV3drs35977759
GWAS Ctlgrs35977759
Max Magnitude0
OMIM142200
Desc
Variant0004
Relatedalso
ClinVar
Risk rs35977759(G;G)
Alt rs35977759(G;G)
Reference rs35977759(A;A)
Significance Other
Disease HEMOGLOBIN F (BONAIRE)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (BONAIRE)
Reversed 1
HGVS NC_000011.9:g.5270794T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016148.1,



[PMID 6186637] Hb F-Bonaire-Ga or alpha 2 A gamma 2 39(C5) Gln replaced by Arg, characterized by high pressure liquid chromatographic and microsequencing procedures.