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rs41475844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs41475844(A;A)
Make rs41475844(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249553
GeneHBG1
is asnp
is mentioned by
dbSNPrs41475844
ebirs41475844
HLIrs41475844
Exacrs41475844
Varsomers41475844
Maprs41475844
PheGenIrs41475844
hapmaprs41475844
1000 genomesrs41475844
hgdprs41475844
ensemblrs41475844
gopubmedrs41475844
geneviewrs41475844
scholarrs41475844
googlers41475844
pharmgkbrs41475844
gwascentralrs41475844
openSNPrs41475844
23andMers41475844
23andMe allrs41475844
SNP Nexus

SNPshotrs41475844
SNPdbers41475844
MSV3drs41475844
GWAS Ctlgrs41475844
Max Magnitude0
OMIM142200
Desc
Variant0010
Relatedalso
ClinVar
Risk rs41475844(A;A)
Alt rs41475844(A;A)
Reference rs41475844(G;G)
Significance Other
Disease HEMOGLOBIN F (FUKUYAMA)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (FUKUYAMA)
Reversed 1
HGVS NC_000011.9:g.5270783C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016154.1,



[PMID 2467893] Hb F-Fukuyama or A gamma T43(CD2)Asp----Asn.