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rs41330850

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs41330850(A;A)
Make rs41330850(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5248418
GeneHBG1
is asnp
is mentioned by
dbSNPrs41330850
ebirs41330850
HLIrs41330850
Exacrs41330850
Varsomers41330850
Maprs41330850
PheGenIrs41330850
hapmaprs41330850
1000 genomesrs41330850
hgdprs41330850
ensemblrs41330850
gopubmedrs41330850
geneviewrs41330850
scholarrs41330850
googlers41330850
pharmgkbrs41330850
gwascentralrs41330850
openSNPrs41330850
23andMers41330850
23andMe allrs41330850
SNP Nexus

SNPshotrs41330850
SNPdbers41330850
MSV3drs41330850
GWAS Ctlgrs41330850
Max Magnitude0
OMIM142200
Desc
Variant0002
Relatedalso


ClinVar
Risk rs41330850(A;A)
Alt rs41330850(A;A)
Reference rs41330850(G;G)
Significance Other
Disease HEMOGLOBIN F (BASKENT)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (BASKENT)
Reversed 1
HGVS NC_000011.9:g.5269648C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016146.1,



[PMID 2454900] Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.