Original source

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

Alleles
-/T
Location

Chromosome 1: between 12196941 and 12196942 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays