Original source

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

Alleles
-/T
Location

Chromosome 14: between 92069372 and 92069373 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs369126323

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 43 transcripts.

Variant displays