Variant Detail

RSID Fallerini_c.901T>C
HGVS GRCh38.p13 chr X_c.901T>C
Chromosome X
Start position12867072
Stop position12890361
Associated gene(s)TLR7
Mutation typeSNP
Reference -
Alternative -
Associated allele -
Associated African Allele Frequency -
Consequence Missense Variant
Other population frequencies linkALFA Fallerini_c.901T>C

Variants

NamePaperDescription of ComparisonGeneRSIDAssociationDisease StatusMAFStatistical Odds RatioStatistical P-value

Papers

Paper