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rs35687396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35687396(A;A)
Make rs35687396(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254652
GeneHBG2
is asnp
is mentioned by
dbSNPrs35687396
ebirs35687396
HLIrs35687396
Exacrs35687396
Varsomers35687396
Maprs35687396
PheGenIrs35687396
hapmaprs35687396
1000 genomesrs35687396
hgdprs35687396
ensemblrs35687396
gopubmedrs35687396
geneviewrs35687396
scholarrs35687396
googlers35687396
pharmgkbrs35687396
gwascentralrs35687396
openSNPrs35687396
23andMers35687396
23andMe allrs35687396
SNP Nexus

SNPshotrs35687396
SNPdbers35687396
MSV3drs35687396
GWAS Ctlgrs35687396
Max Magnitude0
OMIM142250
Desc
Variant0037
Relatedalso
ClinVar
Risk rs35687396(A;A)
Alt rs35687396(A;A)
Reference rs35687396(G;G)
Significance Other
Disease HEMOGLOBIN F (COSENZA)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (COSENZA)
Reversed 1
HGVS NC_000011.9:g.5275882C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016132.1,



[PMID 1726095] Hb F-Cosenza or G gamma 25(B7)Gly----Glu: a new fast-moving fetal hemoglobin variant.