Original source

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

Alleles
-/T
Location

Chromosome 12: between 11667697 and 11667698 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs369062019

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

About this variant

This variant overlaps 4 transcripts.

Variant displays