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rs63751116

From SNPedia

Merged intors35654345
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751116(A;A)
Make rs63751116(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177323
GeneHBA1
is asnp
is mentioned by
dbSNPrs63751116
ebirs63751116
HLIrs63751116
Exacrs63751116
Varsomers63751116
Maprs63751116
PheGenIrs63751116
hapmaprs63751116
1000 genomesrs63751116
hgdprs63751116
ensemblrs63751116
gopubmedrs63751116
geneviewrs63751116
scholarrs63751116
googlers63751116
pharmgkbrs63751116
gwascentralrs63751116
openSNPrs63751116
23andMers63751116
23andMe allrs63751116
SNP Nexus

SNPshotrs63751116
SNPdbers63751116
MSV3drs63751116
GWAS Ctlgrs63751116
StatusMerged into rs35654345
Max Magnitude0
OMIM141800
Desc
Variant0153
Relatedalso
ClinVar
Risk rs63751116(A;A)
Alt rs63751116(A;A)
Reference rs63751116(T;T)
Significance Untested
Disease
Variation info
Gene HBA1
CLNDBN
Reversed 0
HGVS NC_000016.9:g.227322T>A
CLNSRC
CLNACC