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rs41381645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs41381645(A;C)
Make rs41381645(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177018
GeneHBA1
is asnp
is mentioned by
dbSNPrs41381645
ebirs41381645
HLIrs41381645
Exacrs41381645
Varsomers41381645
Maprs41381645
PheGenIrs41381645
hapmaprs41381645
1000 genomesrs41381645
hgdprs41381645
ensemblrs41381645
gopubmedrs41381645
geneviewrs41381645
scholarrs41381645
googlers41381645
pharmgkbrs41381645
gwascentralrs41381645
openSNPrs41381645
23andMers41381645
23andMe allrs41381645
SNP Nexus

SNPshotrs41381645
SNPdbers41381645
MSV3drs41381645
GWAS Ctlgrs41381645
Max Magnitude0
OMIM141800
Desc
Variant0059
Relatedalso
ClinVar
Risk rs41381645(C;C)
Alt rs41381645(C;C)
Reference rs41381645(A;A)
Significance Other
Disease HEMOGLOBIN J (ANATOLIA)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN J (ANATOLIA)
Reversed 0
HGVS NC_000016.9:g.227017A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017058.2,


[PMID 2272835] Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variant.