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rs189600565

From SNPedia

Orientationplus
Stabilizedplus
Make rs189600565(C;C)
Make rs189600565(C;T)
Make rs189600565(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position135097830
is asnp
is mentioned by
dbSNPrs189600565
dbSNP (old)rs189600565
ClinGenrs189600565
ebirs189600565
HLIrs189600565
Exacrs189600565
Gnomadrs189600565
Varsomers189600565
Maprs189600565
PheGenIrs189600565
Biobankrs189600565
1000 genomesrs189600565
hgdprs189600565
ensemblrs189600565
gopubmedrs189600565
geneviewrs189600565
scholarrs189600565
googlers189600565
pharmgkbrs189600565
gwascentralrs189600565
openSNPrs189600565
23andMers189600565
23andMe allrs189600565
SNP Nexus

SNPshotrs189600565
SNPdbers189600565
MSV3drs189600565
GWAS Ctlgrs189600565
Max Magnitude

[PMID 25651163] Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia