Have questions? Visit https://www.reddit.com/r/SNPedia

rs35885783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35885783(A;A)
Make rs35885783(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254504
GeneHBG2
is asnp
is mentioned by
dbSNPrs35885783
ebirs35885783
HLIrs35885783
Exacrs35885783
Varsomers35885783
Maprs35885783
PheGenIrs35885783
hapmaprs35885783
1000 genomesrs35885783
hgdprs35885783
ensemblrs35885783
gopubmedrs35885783
geneviewrs35885783
scholarrs35885783
googlers35885783
pharmgkbrs35885783
gwascentralrs35885783
openSNPrs35885783
23andMers35885783
23andMe allrs35885783
SNP Nexus

SNPshotrs35885783
SNPdbers35885783
MSV3drs35885783
GWAS Ctlgrs35885783
Max Magnitude0
OMIM142250
Desc
Variant0023
Relatedalso
ClinVar
Risk rs35885783(A;A)
Alt rs35885783(A;A)
Reference rs35885783(G;G)
Significance Other
Disease HEMOGLOBIN F (TOKYO)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (TOKYO)
Reversed 1
HGVS NC_000011.9:g.5275734C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016119.1,



[PMID 2581919] Hb F-Tokyo or alpha 2G gamma 2 34(B16)Val----Ile, a silent gamma chain variant detected by reverse phase high performance liquid chromatography.