Have questions? Visit https://www.reddit.com/r/SNPedia

rs35315638

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35315638(G;G)
Make rs35315638(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249796
GeneHBG1
is asnp
is mentioned by
dbSNPrs35315638
ebirs35315638
HLIrs35315638
Exacrs35315638
Varsomers35315638
Maprs35315638
PheGenIrs35315638
hapmaprs35315638
1000 genomesrs35315638
hgdprs35315638
ensemblrs35315638
gopubmedrs35315638
geneviewrs35315638
scholarrs35315638
googlers35315638
pharmgkbrs35315638
gwascentralrs35315638
openSNPrs35315638
23andMers35315638
23andMe allrs35315638
SNP Nexus

SNPshotrs35315638
SNPdbers35315638
MSV3drs35315638
GWAS Ctlgrs35315638
Merged fromRs111033587
Max Magnitude0
OMIM142200
Desc
Variant0035
Relatedalso
ClinVar
Risk rs35315638(G;G)
Alt rs35315638(G;G)
Reference rs35315638(T;T)
Significance Other
Disease HEMOGLOBIN F (MACEDONIA-I)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (MACEDONIA-I)
Reversed 1
HGVS NC_000011.9:g.5271026A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016183.1,



[PMID 7928382] Hb F-Macedonia-I or alpha 2A gamma (2)2(NA2)His- > Gln.