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rs35481866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35481866(A;G)
Make rs35481866(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254407
GeneHBG2
is asnp
is mentioned by
dbSNPrs35481866
ebirs35481866
HLIrs35481866
Exacrs35481866
Varsomers35481866
Maprs35481866
PheGenIrs35481866
hapmaprs35481866
1000 genomesrs35481866
hgdprs35481866
ensemblrs35481866
gopubmedrs35481866
geneviewrs35481866
scholarrs35481866
googlers35481866
pharmgkbrs35481866
gwascentralrs35481866
openSNPrs35481866
23andMers35481866
23andMe allrs35481866
SNP Nexus

SNPshotrs35481866
SNPdbers35481866
MSV3drs35481866
GWAS Ctlgrs35481866
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM142250
Desc
Variant0022
Relatedalso


ClinVar
Risk rs35481866(G,T;G,T)
Alt rs35481866(G,T;G,T)
Reference rs35481866(A;A)
Significance Other
Disease HEMOGLOBIN F (SHANGHAI)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (SHANGHAI)
Reversed 1
HGVS NC_000011.9:g.5275637T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016118.1,



[PMID 2579547] -G gamma A gamma-Thalassemia and gamma-chain variants in Chinese newborn babies.