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rs41416747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs41416747(A;T)
Make rs41416747(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position176955
GeneHBA1
is asnp
is mentioned by
dbSNPrs41416747
dbSNP (classic)rs41416747
ClinGenrs41416747
ebirs41416747
HLIrs41416747
Exacrs41416747
Gnomadrs41416747
Varsomers41416747
LitVarrs41416747
Maprs41416747
PheGenIrs41416747
Biobankrs41416747
1000 genomesrs41416747
hgdprs41416747
ensemblrs41416747
geneviewrs41416747
scholarrs41416747
googlers41416747
pharmgkbrs41416747
gwascentralrs41416747
openSNPrs41416747
23andMers41416747
SNPshotrs41416747
SNPdbers41416747
MSV3drs41416747
GWAS Ctlgrs41416747
Max Magnitude0
OMIM141800
Desc
Variant0169
Relatedalso
ClinVar
Risk rs41416747(C;C) rs41416747(T;T)
Alt rs41416747(C;C) rs41416747(T;T)
Reference Rs41416747(A;A)
Significance Untested
Disease
Variation info
Gene HBA1
CLNDBN
Reversed 0
HGVS NC_000016.9:g.226954A>C; NC_000016.9:g.226954A>T
CLNSRC
CLNACC


[PMID 1634355] Hb Kanagawa [alpha 40(C5)Lys----Met]: a new alpha chain variant with an increased oxygen affinity.