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rs121913128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGT;CGT) 0 common in clinvar
Make rs121913128(-;-)
Make rs121913128(-;CGT)
ReferenceGRCh38 38.1/141
Chromosome16
Position177406
GeneHBA1
is asnp
is mentioned by
dbSNPrs121913128
ebirs121913128
HLIrs121913128
Exacrs121913128
Varsomers121913128
Maprs121913128
PheGenIrs121913128
hapmaprs121913128
1000 genomesrs121913128
hgdprs121913128
ensemblrs121913128
gopubmedrs121913128
geneviewrs121913128
scholarrs121913128
googlers121913128
pharmgkbrs121913128
gwascentralrs121913128
openSNPrs121913128
23andMers121913128
23andMe allrs121913128
SNP Nexus

SNPshotrs121913128
SNPdbers121913128
MSV3drs121913128
GWAS Ctlgrs121913128
Max Magnitude0
OMIM141800
Desc
Variant0083
Relatedalso
ClinVar
Risk rs121913128(;)
Alt rs121913128(;)
Reference rs121913128(CGT;CGT)
Significance Other
Disease HEMOGLOBIN KOELLIKER HEMOGLOBIN F (KOELLIKER)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN KOELLIKER HEMOGLOBIN F (KOELLIKER)
Reversed 0
HGVS NC_000016.9:g.227405_227407delCGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000017081.3, RCV000017082.3,