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rs35654328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35654328(A;A)
Make rs35654328(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254650
GeneHBG2
is asnp
is mentioned by
dbSNPrs35654328
ebirs35654328
HLIrs35654328
Exacrs35654328
Varsomers35654328
Maprs35654328
PheGenIrs35654328
hapmaprs35654328
1000 genomesrs35654328
hgdprs35654328
ensemblrs35654328
gopubmedrs35654328
geneviewrs35654328
scholarrs35654328
googlers35654328
pharmgkbrs35654328
gwascentralrs35654328
openSNPrs35654328
23andMers35654328
23andMe allrs35654328
SNP Nexus

SNPshotrs35654328
SNPdbers35654328
MSV3drs35654328
GWAS Ctlgrs35654328
Max Magnitude0
OMIM142250
Desc
Variant0019
Relatedalso
ClinVar
Risk rs35654328(A;A)
Alt rs35654328(A;A)
Reference rs35654328(G;G)
Significance Other
Disease HEMOGLOBIN F (OAKLAND)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (OAKLAND)
Reversed 1
HGVS NC_000011.9:g.5275880C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016115.1,



[PMID 2442122] Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.