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rs35252931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35252931(C;C)
Make rs35252931(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177005
GeneHBA1
is asnp
is mentioned by
dbSNPrs35252931
ebirs35252931
HLIrs35252931
Exacrs35252931
Varsomers35252931
Maprs35252931
PheGenIrs35252931
hapmaprs35252931
1000 genomesrs35252931
hgdprs35252931
ensemblrs35252931
gopubmedrs35252931
geneviewrs35252931
scholarrs35252931
googlers35252931
pharmgkbrs35252931
gwascentralrs35252931
openSNPrs35252931
23andMers35252931
23andMe allrs35252931
SNP Nexus

SNPshotrs35252931
SNPdbers35252931
MSV3drs35252931
GWAS Ctlgrs35252931
Max Magnitude0
OMIM141800
Desc
Variant0086
Relatedalso
ClinVar
Risk rs35252931(C;C)
Alt rs35252931(C;C)
Reference rs35252931(G;G)
Significance Other
Disease HEMOGLOBIN L (PERSIAN GULF)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN L (PERSIAN GULF)
Reversed 0
HGVS NC_000016.9:g.227004G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017092.2,


[PMID 4982774] Haemoglobin L Persian Gulf: alpha-57 (E6) glycine leads to arginine.