Variant Detail

RSID TLR7 deletion
HGVS NM_016562.3:c.2129_2132del
Chromosome X
Start position12905756
Stop position12905759
Associated gene(s)TLR7
Mutation typeInDel
Reference AACT
Alternative -
Associated allele -
Associated African Allele Frequency none
Consequence Non sense
Other population frequencies linkALFA TLR7 deletion

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper