Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/TTTT
Location

Chromosome 12: between 11667532 and 11667533 (forward strand) | View in location tab

Most severe consequence

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts.

Variation displays