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rs35477770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35477770(C;T)
Make rs35477770(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position176796
GeneHBA1
is asnp
is mentioned by
dbSNPrs35477770
ebirs35477770
HLIrs35477770
Exacrs35477770
Varsomers35477770
Maprs35477770
PheGenIrs35477770
hapmaprs35477770
1000 genomesrs35477770
hgdprs35477770
ensemblrs35477770
gopubmedrs35477770
geneviewrs35477770
scholarrs35477770
googlers35477770
pharmgkbrs35477770
gwascentralrs35477770
openSNPrs35477770
23andMers35477770
23andMe allrs35477770
SNP Nexus

SNPshotrs35477770
SNPdbers35477770
MSV3drs35477770
GWAS Ctlgrs35477770
Max Magnitude0
OMIM141800
Desc
Variant0132
Relatedalso
OMIM141850
Desc
Variant0041
Relatedalso
ClinVar
Risk rs35477770(A,T;A,T)
Alt rs35477770(A,T;A,T)
Reference rs35477770(C;C)
Significance Other
Disease HEMOGLOBIN SHENYANG
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN SHENYANG
Reversed 0
HGVS NC_000016.9:g.226795C>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017153.2,


[PMID 2703370] Hemoglobin Shenyang found among Uygurs in P.R. China.


[PMID 7161109] Hb Shenyang (alpha 26 (B7) Ala replaced by Glu): a new unstable variant found in China.