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rs35723200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35723200(C;C)
Make rs35723200(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position177403
GeneHBA1
is asnp
is mentioned by
dbSNPrs35723200
ebirs35723200
HLIrs35723200
Exacrs35723200
Varsomers35723200
Maprs35723200
PheGenIrs35723200
hapmaprs35723200
1000 genomesrs35723200
hgdprs35723200
ensemblrs35723200
gopubmedrs35723200
geneviewrs35723200
scholarrs35723200
googlers35723200
pharmgkbrs35723200
gwascentralrs35723200
openSNPrs35723200
23andMers35723200
23andMe allrs35723200
SNP Nexus

SNPshotrs35723200
SNPdbers35723200
MSV3drs35723200
GWAS Ctlgrs35723200
Max Magnitude0
OMIM141800
Desc
Variant0182
Relatedalso


ClinVar
Risk rs35723200(C;C)
Alt rs35723200(C;C)
Reference rs35723200(T;T)
Significance Other
Disease HEMOGLOBIN ROUEN HEMOGLOBIN ETHIOPIA
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN ROUEN HEMOGLOBIN ETHIOPIA
Reversed 0
HGVS NC_000016.9:g.227402T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017201.2, RCV000017202.2,



[PMID 1390944] Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity.


[PMID 1428951] Hb Ethiopia or alpha 2(140)(HC2)Tyr----His beta 2.