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

rs35621390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35621390(G;T)
Make rs35621390(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254675
GeneHBG2
is asnp
is mentioned by
dbSNPrs35621390
ebirs35621390
HLIrs35621390
Exacrs35621390
Varsomers35621390
Maprs35621390
PheGenIrs35621390
hapmaprs35621390
1000 genomesrs35621390
hgdprs35621390
ensemblrs35621390
gopubmedrs35621390
geneviewrs35621390
scholarrs35621390
googlers35621390
pharmgkbrs35621390
gwascentralrs35621390
openSNPrs35621390
23andMers35621390
23andMe allrs35621390
SNP Nexus

SNPshotrs35621390
SNPdbers35621390
MSV3drs35621390
GWAS Ctlgrs35621390
Max Magnitude0
OMIM142250
Desc
Variant0048
Relatedalso
ClinVar
Risk rs35621390(C,T;C,T)
Alt rs35621390(C,T;C,T)
Reference rs35621390(G;G)
Significance Other
Disease HEMOGLOBIN F (CLAMART)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (CLAMART)
Reversed 1
HGVS NC_000011.9:g.5275905C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016143.3,


[PMID 10722115] Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys].