Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
-/T
Location

Chromosome 19: between 11380626 and 11380627 (forward strand) | View in location tab

Most severe consequence

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variation displays