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rs281865555

From SNPedia

Orientationplus
Stabilizedplus
Make rs281865555(A;A)
Make rs281865555(A;G)
Make rs281865555(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position172961
GeneHBA2
is asnp
is mentioned by
dbSNPrs281865555
dbSNP (old)rs281865555
ClinGenrs281865555
ebirs281865555
HLIrs281865555
Exacrs281865555
Gnomadrs281865555
Varsomers281865555
Maprs281865555
PheGenIrs281865555
Biobankrs281865555
1000 genomesrs281865555
hgdprs281865555
ensemblrs281865555
gopubmedrs281865555
geneviewrs281865555
scholarrs281865555
googlers281865555
pharmgkbrs281865555
gwascentralrs281865555
openSNPrs281865555
23andMers281865555
23andMe allrs281865555
SNP Nexus

SNPshotrs281865555
SNPdbers281865555
MSV3drs281865555
GWAS Ctlgrs281865555
Max Magnitude
ClinVar
Risk rs281865555(G;G)
Alt rs281865555(G;G)
Reference rs281865555(A;A)
Significance Other
Disease HEMOGLOBIN I HEMOGLOBIN I (BURLINGTON) HEMOGLOBIN I (PHILADELPHIA) HEMOGLOBIN I (SKAMANIA) HEMOGLOBIN I (TEXAS)
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN I HEMOGLOBIN I (BURLINGTON) HEMOGLOBIN I (PHILADELPHIA) HEMOGLOBIN I (SKAMANIA) HEMOGLOBIN I (TEXAS)
Reversed 0
HGVS NC_000016.9:g.222960A>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016905.1, RCV000016906.1, RCV000016907.1, RCV000016908.1, RCV000016909.1,