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rs35548338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35548338(G;G)
Make rs35548338(G;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177093
GeneHBA1
is asnp
is mentioned by
dbSNPrs35548338
ebirs35548338
HLIrs35548338
Exacrs35548338
Varsomers35548338
Maprs35548338
PheGenIrs35548338
hapmaprs35548338
1000 genomesrs35548338
hgdprs35548338
ensemblrs35548338
gopubmedrs35548338
geneviewrs35548338
scholarrs35548338
googlers35548338
pharmgkbrs35548338
gwascentralrs35548338
openSNPrs35548338
23andMers35548338
23andMe allrs35548338
SNP Nexus

SNPshotrs35548338
SNPdbers35548338
MSV3drs35548338
GWAS Ctlgrs35548338
Max Magnitude0
OMIM141800
Desc
Variant0101
Relatedalso


ClinVar
Risk rs35548338(G;G)
Alt rs35548338(G;G)
Reference rs35548338(T;T)
Significance Other
Disease HEMOGLOBIN MOABIT
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN MOABIT
Reversed 0
HGVS NC_000016.9:g.227092T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017117.2,



[PMID 108887] Hemoglobin Moabit: alpha 86 (F7) Leu leads to Arg: a new unstable abnormal hemoglobin.