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rs35957832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35957832(C;C)
Make rs35957832(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249729
GeneHBG1
is asnp
is mentioned by
dbSNPrs35957832
ebirs35957832
HLIrs35957832
Exacrs35957832
Varsomers35957832
Maprs35957832
PheGenIrs35957832
hapmaprs35957832
1000 genomesrs35957832
hgdprs35957832
ensemblrs35957832
gopubmedrs35957832
geneviewrs35957832
scholarrs35957832
googlers35957832
pharmgkbrs35957832
gwascentralrs35957832
openSNPrs35957832
23andMers35957832
23andMe allrs35957832
SNP Nexus

SNPshotrs35957832
SNPdbers35957832
MSV3drs35957832
GWAS Ctlgrs35957832
Max Magnitude0
OMIM142200
Desc
Variant0022
Relatedalso
ClinVar
Risk rs35957832(C;C)
Alt rs35957832(C;C)
Reference rs35957832(G;G)
Significance Other
Disease HEMOGLOBIN F (XINJIANG)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (XINJIANG)
Reversed 1
HGVS NC_000011.9:g.5270959C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016167.2,



[PMID 2448268] Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variant.