Variant Detail

RSID rs334
HGVS NC_000011.9:g.5248232T>A
Chromosome 11
Start position5248232
Stop position5248232
Associated gene(s)HBB
Mutation typeTagged SNP
Reference T
Alternative A/C/G
Associated allele A
Associated African Allele Frequency 0.003
Consequence Missense Variant
Other population frequencies linkALFA rs334

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper