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rs33910377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33910377(C;G)
Make rs33910377(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177326
GeneHBA1
is asnp
is mentioned by
dbSNPrs33910377
ebirs33910377
HLIrs33910377
Exacrs33910377
Varsomers33910377
Maprs33910377
PheGenIrs33910377
hapmaprs33910377
1000 genomesrs33910377
hgdprs33910377
ensemblrs33910377
gopubmedrs33910377
geneviewrs33910377
scholarrs33910377
googlers33910377
pharmgkbrs33910377
gwascentralrs33910377
openSNPrs33910377
23andMers33910377
23andMe allrs33910377
SNP Nexus

SNPshotrs33910377
SNPdbers33910377
MSV3drs33910377
GWAS Ctlgrs33910377
Max Magnitude0
OMIM141800
Desc
Variant0019
Relatedalso
OMIM141800
Desc
Variant0108
Relatedalso
ClinVar
Risk rs33910377(G,T;G,T)
Alt rs33910377(G,T;G,T)
Reference rs33910377(C;C)
Significance Other
Disease HEMOGLOBIN CHIAPAS HEMOGLOBIN NOUAKCHOTT
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN CHIAPAS HEMOGLOBIN NOUAKCHOTT
Reversed 0
HGVS NC_000016.9:g.227325C>G; NC_000016.9:g.227325C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017006.2, RCV000017125.2,


[PMID 5650416] Chemical characterization of hemoglobin-Mexico and hemoglobin-Chiapas.


[PMID 7319830] Hb Chiapas alpha 2 114 Pro replaced by Arg beta 2: identification by high pressure liquid chromatography.


[PMID 2790052] Hemoglobin Nouakchott [alpha 114(GH2)Pro----Leu]: a new hemoglobin variant displaying an unusual increase in hydrophobicity.