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rs41404150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41404150(C;G)
Make rs41404150(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5249573
GeneHBG1
is asnp
is mentioned by
dbSNPrs41404150
ebirs41404150
HLIrs41404150
Exacrs41404150
Varsomers41404150
Maprs41404150
PheGenIrs41404150
hapmaprs41404150
1000 genomesrs41404150
hgdprs41404150
ensemblrs41404150
gopubmedrs41404150
geneviewrs41404150
scholarrs41404150
googlers41404150
pharmgkbrs41404150
gwascentralrs41404150
openSNPrs41404150
23andMers41404150
23andMe allrs41404150
SNP Nexus

SNPshotrs41404150
SNPdbers41404150
MSV3drs41404150
GWAS Ctlgrs41404150
Max Magnitude0
OMIM142200
Desc
Variant0016
Relatedalso
ClinVar
Risk rs41404150(G;G)
Alt rs41404150(G;G)
Reference rs41404150(C;C)
Significance Other
Disease HEMOGLOBIN F (PENDERGRASS)
Variation info
Gene HBG1
CLNDBN HEMOGLOBIN F (PENDERGRASS)
Reversed 1
HGVS NC_000011.9:g.5270803G>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016160.1,



[PMID 2581920] Hb F-Pendergrass, an A gamma I variant with a Pro----Arg substitution at position gamma 36(C2).