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rs35521813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs35521813(A;C)
Make rs35521813(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254704
GeneHBG2
is asnp
is mentioned by
dbSNPrs35521813
ebirs35521813
HLIrs35521813
Exacrs35521813
Varsomers35521813
Maprs35521813
PheGenIrs35521813
hapmaprs35521813
1000 genomesrs35521813
hgdprs35521813
ensemblrs35521813
gopubmedrs35521813
geneviewrs35521813
scholarrs35521813
googlers35521813
pharmgkbrs35521813
gwascentralrs35521813
openSNPrs35521813
23andMers35521813
23andMe allrs35521813
SNP Nexus

SNPshotrs35521813
SNPdbers35521813
MSV3drs35521813
GWAS Ctlgrs35521813
Max Magnitude0
OMIM142250
Desc
Variant0001
Relatedalso
ClinVar
Risk rs35521813(C,G;C,G)
Alt rs35521813(C,G;C,G)
Reference rs35521813(A;A)
Significance Other
Disease HEMOGLOBIN F (ALBAICIN)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (ALBAICIN)
Reversed 1
HGVS NC_000011.9:g.5275934T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016097.2,


[PMID 2435680] Hb F-Albaicin or G gamma 8(A5)Lys----Glu or Gln.