Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/TTTT/TT/T|MAF: 0.43 (T)
Location

Chromosome 11: between 47439712 and 47439713 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2504 sample genotypes.

Variant displays