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rs35959442

From SNPedia

Orientationplus
Stabilizedplus
Make rs35959442(C;C)
Make rs35959442(C;G)
Make rs35959442(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position135103041
is asnp
is mentioned by
dbSNPrs35959442
ebirs35959442
HLIrs35959442
Exacrs35959442
Varsomers35959442
Maprs35959442
PheGenIrs35959442
hapmaprs35959442
1000 genomesrs35959442
hgdprs35959442
ensemblrs35959442
gopubmedrs35959442
geneviewrs35959442
scholarrs35959442
googlers35959442
pharmgkbrs35959442
gwascentralrs35959442
openSNPrs35959442
23andMers35959442
23andMe allrs35959442
SNP Nexus

SNPshotrs35959442
SNPdbers35959442
MSV3drs35959442
GWAS Ctlgrs35959442
GMAF0.3044
Max Magnitude

[PMID 22191716] Analysis of the rs35959442 Polymorphism in Hb E/?-Thalassemia in Guangxi Province of the People's Republic of China[PMID 19148297OA-icon.png] Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.