Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/TTTT/TT
Location

Chromosome 11: between 47461263 and 47461264 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays