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rs63750388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750388(C;G)
Make rs63750388(G;G)
ReferenceGRCh37 37.1/132
Chromosome16
Position227325
GeneHBA1
is asnp
is mentioned by
dbSNPrs63750388
ebirs63750388
HLIrs63750388
Exacrs63750388
Varsomers63750388
Maprs63750388
PheGenIrs63750388
hapmaprs63750388
1000 genomesrs63750388
hgdprs63750388
ensemblrs63750388
gopubmedrs63750388
geneviewrs63750388
scholarrs63750388
googlers63750388
pharmgkbrs63750388
gwascentralrs63750388
openSNPrs63750388
23andMers63750388
23andMe allrs63750388
SNP Nexus

SNPshotrs63750388
SNPdbers63750388
MSV3drs63750388
GWAS Ctlgrs63750388
StatusDeleted
Max Magnitude0
OMIM141800
Desc
Variant0019
Relatedalso
OMIM141800
Desc
Variant0108
Relatedalso
ClinVar
Risk rs63750388(G,T;G,T)
Alt rs63750388(G,T;G,T)
Reference rs63750388(C;C)
Significance Untested
Disease
Variation info
Gene HBA1
CLNDBN
Reversed 0
HGVS NC_000016.9:g.227325C>G; NC_000016.9:g.227325C>T
CLNSRC
CLNACC