Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs63751308(A;C)
Make rs63751308(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177365
GeneHBA1
is asnp
is mentioned by
dbSNPrs63751308
ebirs63751308
HLIrs63751308
Exacrs63751308
Varsomers63751308
Maprs63751308
PheGenIrs63751308
hapmaprs63751308
1000 genomesrs63751308
hgdprs63751308
ensemblrs63751308
gopubmedrs63751308
geneviewrs63751308
scholarrs63751308
googlers63751308
pharmgkbrs63751308
gwascentralrs63751308
openSNPrs63751308
23andMers63751308
23andMe allrs63751308
SNP Nexus

SNPshotrs63751308
SNPdbers63751308
MSV3drs63751308
GWAS Ctlgrs63751308
Max Magnitude0
OMIM141800
Desc
Variant0137
Relatedalso
ClinVar
Risk rs63751308(C;C)
Alt rs63751308(C;C)
Reference rs63751308(A;A)
Significance Other
Disease HEMOGLOBIN ST. CLAUDE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN ST. CLAUDE
Reversed 0
HGVS NC_000016.9:g.227364A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017158.2,


[PMID 4429670] Hemoglobin St. Claude or alpha2-127(H10)Lys leads to Thr-beta2.