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rs35973315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35973315(A;G)
Make rs35973315(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226773
GeneHBB
is asnp
is mentioned by
dbSNPrs35973315
ebirs35973315
HLIrs35973315
Exacrs35973315
Varsomers35973315
Maprs35973315
PheGenIrs35973315
hapmaprs35973315
1000 genomesrs35973315
hgdprs35973315
ensemblrs35973315
gopubmedrs35973315
geneviewrs35973315
scholarrs35973315
googlers35973315
pharmgkbrs35973315
gwascentralrs35973315
openSNPrs35973315
23andMers35973315
23andMe allrs35973315
SNP Nexus

SNPshotrs35973315
SNPdbers35973315
MSV3drs35973315
GWAS Ctlgrs35973315
Max Magnitude0
OMIM141900
Desc
Variant0282
Relatedalso


ClinVar
Risk rs35973315(G;G)
Alt rs35973315(G;G)
Reference rs35973315(A;A)
Significance Other
Disease HEMOGLOBIN TIANSHUI
Variation info
Gene HBB
CLNDBN HEMOGLOBIN TIANSHUI
Reversed 1
HGVS NC_000011.9:g.5248003T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016624.4,



[PMID 2079437] A new slow-moving hemoglobin variant Hb Tianshui or alpha 2 beta(2)39(C5)Gln----Arg, observed in a Chinese family living in Gansu.