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rs41514946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41514946(A;A)
Make rs41514946(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173573
GeneHBA2
is asnp
is mentioned by
dbSNPrs41514946
ebirs41514946
HLIrs41514946
Exacrs41514946
Varsomers41514946
Maprs41514946
PheGenIrs41514946
hapmaprs41514946
1000 genomesrs41514946
hgdprs41514946
ensemblrs41514946
gopubmedrs41514946
geneviewrs41514946
scholarrs41514946
googlers41514946
pharmgkbrs41514946
gwascentralrs41514946
openSNPrs41514946
23andMers41514946
23andMe allrs41514946
SNP Nexus

SNPshotrs41514946
SNPdbers41514946
MSV3drs41514946
GWAS Ctlgrs41514946
Max Magnitude0
OMIM141850
Desc
Variant0062
Relatedalso
ClinVar
Risk rs41514946(A,G;A,G)
Alt rs41514946(A,G;A,G)
Reference rs41514946(C;C)
Significance Other
Disease Hemoglobin Val de Marne
Variation info
Gene HBA2
CLNDBN Hemoglobin Val de Marne
Reversed 0
HGVS NC_000016.9:g.223572C>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016974.2,