Variant Detail

RSID rs148218440
HGVS NC_000019.9:g.29589778G>A
Chromosome 19
Start position29589778
Stop position29589778
Associated gene(s)UQCRFS1/LOC105372352
Mutation typeTagged SNP
Reference G
Alternative A
Associated allele A
Associated African Allele Frequency 0.0255
Consequence Intergenic
Other population frequencies linkALFA rs148218440

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper