Original source

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

Alleles
-/GTAAGCTATTAAAAAAAGG/TAAGCTATTAAAAAAAGGG
Location

Chromosome 14: between 35402236 and 35402237 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs147444522

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 1 sample genotype.

Variant displays